Canonical Allele Identifier: CA15635633
Gene: ABLIM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114445017A>G , CM000672.2:g.114445017A>G GRCh38
NC_000010.10:g.116204776A>G , CM000672.1:g.116204776A>G GRCh37
NC_000010.9:g.116194766A>G NCBI36
NG_029872.1:g.244639T>C
NG_029872.2:g.381627T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651023.2:c.1458+295T>C ENSP00000499023.2:n.1458+295T>C
ENST00000707119.1:c.1353+295T>C ENSP00000516747.1:n.1353+295T>C
ENST00000533213.7:c.1827+295T>C MANE Select ENSP00000433629.3:n.1827+295T>C
ENST00000649363.1:c.1995+295T>C ENSP00000497150.1:n.1995+295T>C
ENST00000651023.1:c.1458+295T>C ENSP00000499023.1:n.1458+295T>C
ENST00000651092.1:c.1230+295T>C ENSP00000499163.1:n.1230+295T>C
ENST00000277895.9:c.1827+295T>C ENSP00000277895.5:n.1827+295T>C
ENST00000369252.8:c.1731+295T>C ENSP00000358256.5:n.1731+295T>C
ENST00000369253.6:c.696+295T>C ENSP00000358257.2:n.696+295T>C
ENST00000369256.6:c.1737+295T>C ENSP00000358260.3:n.1737+295T>C
ENST00000369266.7:c.696+295T>C ENSP00000358270.4:n.696+295T>C
ENST00000392952.7:c.858+295T>C ENSP00000376679.3:n.858+295T>C
ENST00000392955.7:c.1647+295T>C ENSP00000376682.4:n.1647+295T>C
ENST00000533213.6:c.1647+295T>C ENSP00000433629.2:n.1647+295T>C
NM_001003407.1:c.1647+295T>C NP_001003407.1:n.1647+295T>C
NM_001003408.1:c.1731+295T>C NP_001003408.1:n.1731+295T>C
NM_002313.5:c.1827+295T>C NP_002304.3:n.1827+295T>C
NM_006720.3:c.858+295T>C NP_006711.3:n.858+295T>C
XM_005269818.1:c.1737+295T>C XP_005269875.1:n.1737+295T>C
XM_005269824.1:c.1458+295T>C XP_005269881.1:n.1458+295T>C
XM_005269826.1:c.1089+295T>C XP_005269883.1:n.1089+295T>C
XM_005269827.3:c.1005+295T>C XP_005269884.1:n.1005+295T>C
XM_005269828.3:c.774+295T>C XP_005269885.1:n.774+295T>C
XM_005269830.3:c.633+295T>C XP_005269887.1:n.633+295T>C
XM_006717837.1:c.1857+295T>C XP_006717900.1:n.1857+295T>C
XM_006717838.1:c.1809+295T>C XP_006717901.1:n.1809+295T>C
XM_006717846.2:c.1089+295T>C XP_006717909.1:n.1089+295T>C
XM_006717847.1:c.1005+295T>C XP_006717910.1:n.1005+295T>C
XM_006717848.1:c.780+295T>C XP_006717911.1:n.780+295T>C
XM_011539801.1:c.1896+295T>C XP_011538103.1:n.1896+295T>C
XM_011539802.1:c.1809+295T>C XP_011538104.1:n.1809+295T>C
XM_011539803.1:c.1788+295T>C XP_011538105.1:n.1788+295T>C
XM_011539804.1:c.1266+295T>C XP_011538106.1:n.1266+295T>C
XM_011539805.1:c.1581+295T>C XP_011538107.1:n.1581+295T>C
XM_011539806.1:c.1125+295T>C XP_011538108.1:n.1125+295T>C
NM_001322882.2:c.1737+295T>C NP_001309811.1:n.1737+295T>C
NM_001322883.1:c.1542+295T>C NP_001309812.1:n.1542+295T>C
NM_001322884.2:c.1497+295T>C NP_001309813.1:n.1497+295T>C
NM_001322885.2:c.1491+295T>C NP_001309814.1:n.1491+295T>C
NM_001322886.2:c.1455+295T>C NP_001309815.1:n.1455+295T>C
NM_001322887.1:c.1401+295T>C NP_001309816.1:n.1401+295T>C
NM_001322888.1:c.858+295T>C NP_001309817.1:n.858+295T>C
NM_001322889.1:c.822+295T>C NP_001309818.1:n.822+295T>C
NM_001322890.1:c.780+295T>C NP_001309819.1:n.780+295T>C
NM_001322891.1:c.780+295T>C NP_001309820.1:n.780+295T>C
NM_001322892.1:c.774+295T>C NP_001309821.1:n.774+295T>C
NM_001322893.1:c.774+295T>C NP_001309822.1:n.774+295T>C
NM_001322894.1:c.738+295T>C NP_001309823.1:n.738+295T>C
NM_001322895.1:c.738+295T>C NP_001309824.1:n.738+295T>C
NM_001322896.1:c.696+295T>C NP_001309825.1:n.696+295T>C
NM_001322897.1:c.660+295T>C NP_001309826.1:n.660+295T>C
NM_001322898.1:c.633+295T>C NP_001309827.1:n.633+295T>C
NM_001322899.1:c.633+295T>C NP_001309828.1:n.633+295T>C
NM_001322900.1:c.555+295T>C NP_001309829.1:n.555+295T>C
NM_001352440.1:c.1458+295T>C NP_001339369.1:n.1458+295T>C
NM_001352441.1:c.1353+295T>C NP_001339370.1:n.1353+295T>C
NM_001352442.1:c.1266+295T>C NP_001339371.1:n.1266+295T>C
NM_001352443.1:c.885+295T>C NP_001339372.1:n.885+295T>C
NM_002313.6:c.1827+295T>C NP_002304.3:n.1827+295T>C
XM_005269827.4:c.1005+295T>C XP_005269884.1:n.1005+295T>C
XM_006717837.2:c.1857+295T>C XP_006717900.1:n.1857+295T>C
XM_006717846.3:c.1089+295T>C XP_006717909.1:n.1089+295T>C
XM_011539801.2:c.1581+295T>C XP_011538103.2:n.1581+295T>C
XM_011539802.2:c.1827+295T>C XP_011538104.2:n.1827+295T>C
XM_017016245.1:c.1806+295T>C XP_016871734.1:n.1806+295T>C
XM_017016247.1:c.1350+295T>C XP_016871736.1:n.1350+295T>C
XM_017016248.1:c.1350+295T>C XP_016871737.1:n.1350+295T>C
XM_017016250.1:c.1722+295T>C XP_016871739.1:n.1722+295T>C
XM_017016255.1:c.1602+295T>C XP_016871744.1:n.1602+295T>C
XM_017016256.1:c.1500+295T>C XP_016871745.1:n.1500+295T>C
XM_017016259.1:c.885+295T>C XP_016871748.1:n.885+295T>C
XM_024448010.1:c.1575+295T>C XP_024303778.1:n.1575+295T>C
XM_024448011.1:c.1455+295T>C XP_024303779.1:n.1455+295T>C
XM_024448012.1:c.1434+295T>C XP_024303780.1:n.1434+295T>C
XM_024448013.1:c.1497+295T>C XP_024303781.1:n.1497+295T>C
XM_024448014.1:c.1809+295T>C XP_024303782.1:n.1809+295T>C
XM_024448015.1:c.1314+295T>C XP_024303783.1:n.1314+295T>C
XM_024448016.1:c.1725+295T>C XP_024303784.1:n.1725+295T>C
XM_024448017.1:c.1209+295T>C XP_024303785.1:n.1209+295T>C
XM_024448018.1:c.1584+295T>C XP_024303786.1:n.1584+295T>C
XM_024448020.1:c.1230+295T>C XP_024303788.1:n.1230+295T>C
XM_024448021.1:c.1125+295T>C XP_024303789.1:n.1125+295T>C
XM_024448022.1:c.879+295T>C XP_024303790.1:n.879+295T>C
NM_001003407.2:c.1647+295T>C NP_001003407.1:n.1647+295T>C
NM_001322883.2:c.1542+295T>C NP_001309812.1:n.1542+295T>C
NM_001322884.3:c.1497+295T>C NP_001309813.1:n.1497+295T>C
NM_001322885.3:c.1491+295T>C NP_001309814.1:n.1491+295T>C
NM_001322886.3:c.1455+295T>C NP_001309815.1:n.1455+295T>C
NM_001322887.2:c.1401+295T>C NP_001309816.1:n.1401+295T>C
NM_001322888.2:c.858+295T>C NP_001309817.1:n.858+295T>C
NM_001322889.2:c.822+295T>C NP_001309818.1:n.822+295T>C
NM_001322890.2:c.780+295T>C NP_001309819.1:n.780+295T>C
NM_001322891.2:c.780+295T>C NP_001309820.1:n.780+295T>C
NM_001322892.2:c.774+295T>C NP_001309821.1:n.774+295T>C
NM_001322893.2:c.774+295T>C NP_001309822.1:n.774+295T>C
NM_001322894.2:c.738+295T>C NP_001309823.1:n.738+295T>C
NM_001322895.2:c.738+295T>C NP_001309824.1:n.738+295T>C
NM_001322896.2:c.696+295T>C NP_001309825.1:n.696+295T>C
NM_001322897.2:c.660+295T>C NP_001309826.1:n.660+295T>C
NM_001322898.2:c.633+295T>C NP_001309827.1:n.633+295T>C
NM_001322899.2:c.633+295T>C NP_001309828.1:n.633+295T>C
NM_001322900.2:c.555+295T>C NP_001309829.1:n.555+295T>C
NM_001352442.2:c.1266+295T>C NP_001339371.1:n.1266+295T>C
NM_001352443.2:c.885+295T>C NP_001339372.1:n.885+295T>C
NM_002313.7:c.1827+295T>C MANE Select NP_002304.3:n.1827+295T>C
NM_006720.4:c.858+295T>C NP_006711.3:n.858+295T>C