Canonical Allele Identifier: CA214568098
Gene: ABLIM1 HGNC NCBI

Linked Data

dbSNP Id: rs10885582

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114567791T>C , CM000672.2:g.114567791T>C GRCh38
NC_000010.10:g.116327550T>C , CM000672.1:g.116327550T>C GRCh37
NC_000010.9:g.116317540T>C NCBI36
NG_029872.1:g.121865A>G
NG_029872.2:g.258853A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651023.2:c.445+3506A>G ENSP00000499023.2:n.445+3506A>G
ENST00000707119.1:c.445+3506A>G ENSP00000516747.1:n.445+3506A>G
ENST00000533213.7:c.673+3506A>G MANE Select ENSP00000433629.3:n.673+3506A>G
ENST00000649363.1:c.673+3506A>G ENSP00000497150.1:n.673+3506A>G
ENST00000651023.1:c.445+3506A>G ENSP00000499023.1:n.445+3506A>G
ENST00000651092.1:c.217+3506A>G ENSP00000499163.1:n.217+3506A>G
ENST00000277895.9:c.673+3506A>G ENSP00000277895.5:n.673+3506A>G
ENST00000369252.8:c.493+3506A>G ENSP00000358256.5:n.493+3506A>G
ENST00000369256.6:c.493+3506A>G ENSP00000358260.3:n.493+3506A>G
ENST00000392955.7:c.493+3506A>G ENSP00000376682.4:n.493+3506A>G
ENST00000481974.1:n.232+3506A>G
ENST00000533213.6:c.493+3506A>G ENSP00000433629.2:n.493+3506A>G
NM_001003407.1:c.493+3506A>G NP_001003407.1:n.493+3506A>G
NM_001003408.1:c.493+3506A>G NP_001003408.1:n.493+3506A>G
NM_002313.5:c.673+3506A>G NP_002304.3:n.673+3506A>G
XM_005269818.1:c.493+3506A>G XP_005269875.1:n.493+3506A>G
XM_005269824.1:c.445+3506A>G XP_005269881.1:n.445+3506A>G
XM_006717837.1:c.493+3506A>G XP_006717900.1:n.493+3506A>G
XM_006717838.1:c.445+3506A>G XP_006717901.1:n.445+3506A>G
XM_011539801.1:c.532+3506A>G XP_011538103.1:n.532+3506A>G
XM_011539802.1:c.445+3506A>G XP_011538104.1:n.445+3506A>G
XM_011539803.1:c.634+3506A>G XP_011538105.1:n.634+3506A>G
XM_011539804.1:c.217+3506A>G XP_011538106.1:n.217+3506A>G
XM_011539805.1:c.217+3506A>G XP_011538107.1:n.217+3506A>G
XM_011539806.1:c.217+3506A>G XP_011538108.1:n.217+3506A>G
NM_001322882.2:c.493+3506A>G NP_001309811.1:n.493+3506A>G
NM_001322883.1:c.493+3506A>G NP_001309812.1:n.493+3506A>G
NM_001322884.2:c.442+3506A>G NP_001309813.1:n.442+3506A>G
NM_001322885.2:c.442+3506A>G NP_001309814.1:n.442+3506A>G
NM_001322886.2:c.442+3506A>G NP_001309815.1:n.442+3506A>G
NM_001322887.1:c.493+3506A>G NP_001309816.1:n.493+3506A>G
NM_001352440.1:c.445+3506A>G NP_001339369.1:n.445+3506A>G
NM_001352441.1:c.445+3506A>G NP_001339370.1:n.445+3506A>G
NM_001352442.1:c.217+3506A>G NP_001339371.1:n.217+3506A>G
NM_002313.6:c.673+3506A>G NP_002304.3:n.673+3506A>G
XM_006717837.2:c.493+3506A>G XP_006717900.1:n.493+3506A>G
XM_011539801.2:c.217+3506A>G XP_011538103.2:n.217+3506A>G
XM_011539802.2:c.463+3506A>G XP_011538104.2:n.463+3506A>G
XM_017016245.1:c.442+3506A>G XP_016871734.1:n.442+3506A>G
XM_017016247.1:c.217+3506A>G XP_016871736.1:n.217+3506A>G
XM_017016248.1:c.217+3506A>G XP_016871737.1:n.217+3506A>G
XM_017016250.1:c.442+3506A>G XP_016871739.1:n.442+3506A>G
XM_017016255.1:c.442+3506A>G XP_016871744.1:n.442+3506A>G
XM_017016256.1:c.445+3506A>G XP_016871745.1:n.445+3506A>G
XM_024448010.1:c.217+3506A>G XP_024303778.1:n.217+3506A>G
XM_024448011.1:c.217+3506A>G XP_024303779.1:n.217+3506A>G
XM_024448012.1:c.217+3506A>G XP_024303780.1:n.217+3506A>G
XM_024448013.1:c.217+3506A>G XP_024303781.1:n.217+3506A>G
XM_024448014.1:c.445+3506A>G XP_024303782.1:n.445+3506A>G
XM_024448015.1:c.217+3506A>G XP_024303783.1:n.217+3506A>G
XM_024448016.1:c.445+3506A>G XP_024303784.1:n.445+3506A>G
XM_024448017.1:c.217+3506A>G XP_024303785.1:n.217+3506A>G
XM_024448018.1:c.445+3506A>G XP_024303786.1:n.445+3506A>G
XM_024448019.1:c.217+3506A>G XP_024303787.1:n.217+3506A>G
XM_024448020.1:c.217+3506A>G XP_024303788.1:n.217+3506A>G
XM_024448021.1:c.217+3506A>G XP_024303789.1:n.217+3506A>G
NM_001003407.2:c.493+3506A>G NP_001003407.1:n.493+3506A>G
NM_001322883.2:c.493+3506A>G NP_001309812.1:n.493+3506A>G
NM_001322884.3:c.442+3506A>G NP_001309813.1:n.442+3506A>G
NM_001322885.3:c.442+3506A>G NP_001309814.1:n.442+3506A>G
NM_001322886.3:c.442+3506A>G NP_001309815.1:n.442+3506A>G
NM_001322887.2:c.493+3506A>G NP_001309816.1:n.493+3506A>G
NM_001352442.2:c.217+3506A>G NP_001339371.1:n.217+3506A>G
NM_002313.7:c.673+3506A>G MANE Select NP_002304.3:n.673+3506A>G