Canonical Allele Identifier: CA1539667502
Gene: CPLANE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37125134T= , CM000667.2:g.37125134T= GRCh38
NC_000005.9:g.37125236T= , CM000667.1:g.37125236T= GRCh37
NC_000005.8:g.37160993T= NCBI36
NG_032772.1:g.129295A=
NG_032772.2:g.129295A=

Transcript Alleles

HGVS Amino-acid change
ENST00000510830.2:n.2067A=
ENST00000651892.2:c.8958+110A= MANE Select ENSP00000498265.2:n.8958+110A=
ENST00000676160.1:n.819+110A=
ENST00000425232.6:c.8796+110A= ENSP00000389014.2:n.8796+110A=
ENST00000508244.5:c.8796+110A= ENSP00000421690.1:n.8796+110A=
ENST00000509849.5:c.5970+110A= ENSP00000426337.1:n.5970+110A=
ENST00000509957.5:n.4139+110A=
ENST00000512288.5:n.342-3350A=
ENST00000514429.5:c.5994+110A= ENSP00000424223.1:n.5994+110A=
NM_023073.3:c.8796+110A= NP_075561.3:n.8796+110A=
XM_005248345.2:c.8958+110A= XP_005248402.1:n.8958+110A=
XM_005248346.2:c.8955+110A= XP_005248403.1:n.8955+110A=
XM_005248347.2:c.8955+110A= XP_005248404.1:n.8955+110A=
XM_005248349.2:c.8847+110A= XP_005248406.1:n.8847+110A=
XM_005248350.2:c.8829+110A= XP_005248407.1:n.8829+110A=
XM_005248353.3:c.5601+110A= XP_005248410.1:n.5601+110A=
XM_006714489.2:c.8958+110A= XP_006714552.1:n.8958+110A=
XM_006714491.2:c.3531+110A= XP_006714554.1:n.3531+110A=
XM_011514085.1:c.8958+110A= XP_011512387.1:n.8958+110A=
XM_011514086.1:c.8958+110A= XP_011512388.1:n.8958+110A=
XM_011514087.1:c.8904+110A= XP_011512389.1:n.8904+110A=
XM_011514088.1:c.8850+110A= XP_011512390.1:n.8850+110A=
XM_011514089.1:c.8958+110A= XP_011512391.1:n.8958+110A=
XM_011514090.1:c.8640+110A= XP_011512392.1:n.8640+110A=
XM_011514091.1:c.8286+110A= XP_011512393.1:n.8286+110A=
XM_011514092.1:c.8958+110A= XP_011512394.1:n.8958+110A=
XM_011514094.1:c.6183+110A= XP_011512396.1:n.6183+110A=
XR_427661.2:n.9133+110A=
XR_925644.1:n.9133+110A=
XM_005248345.4:c.8958+110A= XP_005248402.1:n.8958+110A=
XM_005248346.4:c.8955+110A= XP_005248403.1:n.8955+110A=
XM_005248347.4:c.8955+110A= XP_005248404.1:n.8955+110A=
XM_005248349.4:c.8847+110A= XP_005248406.1:n.8847+110A=
XM_005248350.4:c.8829+110A= XP_005248407.1:n.8829+110A=
XM_006714491.3:c.3531+110A= XP_006714554.1:n.3531+110A=
XM_011514085.3:c.8958+110A= XP_011512387.1:n.8958+110A=
XM_011514086.3:c.8958+110A= XP_011512388.1:n.8958+110A=
XM_011514087.2:c.8904+110A= XP_011512389.1:n.8904+110A=
XM_011514088.2:c.8850+110A= XP_011512390.1:n.8850+110A=
XM_011514089.2:c.8958+110A= XP_011512391.1:n.8958+110A=
XM_011514090.3:c.8640+110A= XP_011512392.1:n.8640+110A=
XM_011514092.2:c.8958+110A= XP_011512394.1:n.8958+110A=
XM_011514094.2:c.6183+110A= XP_011512396.1:n.6183+110A=
XM_017009760.1:c.8769+110A= XP_016865249.1:n.8769+110A=
XM_017009761.2:c.8769+110A= XP_016865250.1:n.8769+110A=
XM_017009763.1:c.7965+110A= XP_016865252.1:n.7965+110A=
XM_017009765.1:c.7770+110A= XP_016865254.1:n.7770+110A=
XM_017009766.1:c.5601+110A= XP_016865255.1:n.5601+110A=
XM_024446183.1:c.8769+110A= XP_024301951.1:n.8769+110A=
XM_024446184.1:c.8640+110A= XP_024301952.1:n.8640+110A=
XM_024446185.1:c.8286+110A= XP_024301953.1:n.8286+110A=
XM_024446186.1:c.7965+110A= XP_024301954.1:n.7965+110A=
XR_925644.2:n.9182+110A=
NM_001384732.1:c.8958+110A= MANE Select NP_001371661.1:n.8958+110A=
NM_023073.4:c.8796+110A= NP_075561.3:n.8796+110A=