Canonical Allele Identifier: CA2306109019
Gene: ATP8B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.57688298C= , CM000680.2:g.57688298C= GRCh38
NC_000018.9:g.55355530C= , CM000680.1:g.55355530C= GRCh37
NC_000018.8:g.53506528C= NCBI36
NG_007148.2:g.119798G=
NG_007148.3:g.120525G=

Transcript Alleles

HGVS Amino-acid change
ENST00000642462.1:c.1429+1G= ENSP00000494712.1:n.1429+1G=
ENST00000648039.1:c.1429+1G= ENSP00000497863.1:n.1429+1G=
ENST00000648467.1:c.1262+1G=
ENST00000648908.2:c.1429+1G= MANE Select ENSP00000497896.1:n.1429+1G=
ENST00000283684.8:c.1429+1G= ENSP00000283684.4:n.1429+1G=
ENST00000536015.5:c.1429+1G= ENSP00000445359.1:n.1429+1G=
ENST00000588255.1:c.157+1G= ENSP00000468266.1:n.157+1G=
NM_005603.4:c.1429+1G= NP_005594.1:n.1429+1G=
XM_006722481.2:c.1429+1G= XP_006722544.1:n.1429+1G=
XM_011526020.1:c.1429+1G= XP_011524322.1:n.1429+1G=
XM_011526021.1:c.1429+1G= XP_011524323.1:n.1429+1G=
XM_011526022.1:c.1429+1G= XP_011524324.1:n.1429+1G=
XM_011526023.1:c.1315+1G= XP_011524325.1:n.1315+1G=
XM_011526024.1:c.709+1G= XP_011524326.1:n.709+1G=
XR_935525.1:n.31+1715C=
XR_935526.1:n.31+1715C=
NM_005603.6:c.1429+1G= NP_005594.2:n.1429+1G=
XM_006722481.4:c.1429+1G= XP_006722544.1:n.1429+1G=
XM_011526023.3:c.1315+1G= XP_011524325.1:n.1315+1G=
NM_001374385.1:c.1429+1G= MANE Select NP_001361314.1:n.1429+1G=
NM_001374386.1:c.1279+1G= NP_001361315.1:n.1279+1G=