Canonical Allele Identifier: CA2306103192
Gene: ATP8B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.57674985_57674986delinsAC , CM000680.2:g.57674985_57674986delinsAC GRCh38
NC_000018.9:g.55342217_55342218delinsAC , CM000680.1:g.55342217_55342218delinsAC GRCh37
NC_000018.8:g.53493215_53493216delinsAC NCBI36
NG_007148.2:g.133110_133111delinsGT
NG_007148.3:g.133837_133838delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000642462.1:c.1667_1668delinsGT ENSP00000494712.1:p.Gly556=
ENST00000648039.1:c.1667_1668delinsGT ENSP00000497863.1:p.Gly556=
ENST00000648467.1:c.1532_1533delinsGT
ENST00000648908.2:c.1667_1668delinsGT MANE Select ENSP00000497896.1:p.Gly556=
ENST00000283684.8:c.1667_1668delinsGT ENSP00000283684.4:p.Gly556=
ENST00000536015.5:c.1667_1668delinsGT ENSP00000445359.1:p.Gly556=
NM_005603.4:c.1667_1668delinsGT NP_005594.1:p.Gly556=
XM_006722481.2:c.1667_1668delinsGT XP_006722544.1:p.Gly556=
XM_011526020.1:c.1667_1668delinsGT XP_011524322.1:p.Gly556=
XM_011526021.1:c.1667_1668delinsGT XP_011524323.1:p.Gly556=
XM_011526022.1:c.1667_1668delinsGT XP_011524324.1:p.Gly556=
XM_011526023.1:c.1553_1554delinsGT XP_011524325.1:p.Gly518=
XM_011526024.1:c.947_948delinsGT XP_011524326.1:p.Gly316=
NM_005603.6:c.1667_1668delinsGT NP_005594.2:p.Gly556=
XM_006722481.4:c.1667_1668delinsGT XP_006722544.1:p.Gly556=
XM_011526023.3:c.1553_1554delinsGT XP_011524325.1:p.Gly518=
NM_001374385.1:c.1667_1668delinsGT MANE Select NP_001361314.1:p.Gly556=
NM_001374386.1:c.1517_1518delinsGT NP_001361315.1:p.Gly506=