Canonical Allele Identifier: CA2306103178

Gene: ATP8B1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57674952A= , CM000680.2:g.57674952A=	GRCh38
NC_000018.9:g.55342184A= , CM000680.1:g.55342184A=	GRCh37
NC_000018.8:g.53493182A=	NCBI36
NG_007148.2:g.133144T=
NG_007148.3:g.133871T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642462.1:c.1701T=	ENSP00000494712.1:p.Phe567=
ENST00000648039.1:c.1701T=	ENSP00000497863.1:p.Phe567=
ENST00000648467.1:c.1566T=
ENST00000648908.2:c.1701T= MANE Select	ENSP00000497896.1:p.Phe567=
ENST00000283684.8:c.1701T=	ENSP00000283684.4:p.Phe567=
ENST00000536015.5:c.1701T=	ENSP00000445359.1:p.Phe567=
NM_005603.4:c.1701T=	NP_005594.1:p.Phe567=
XM_006722481.2:c.1701T=	XP_006722544.1:p.Phe567=
XM_011526020.1:c.1701T=	XP_011524322.1:p.Phe567=
XM_011526021.1:c.1701T=	XP_011524323.1:p.Phe567=
XM_011526022.1:c.1701T=	XP_011524324.1:p.Phe567=
XM_011526023.1:c.1587T=	XP_011524325.1:p.Phe529=
XM_011526024.1:c.981T=	XP_011524326.1:p.Phe327=
NM_005603.6:c.1701T=	NP_005594.2:p.Phe567=
XM_006722481.4:c.1701T=	XP_006722544.1:p.Phe567=
XM_011526023.3:c.1587T=	XP_011524325.1:p.Phe529=
NM_001374385.1:c.1701T= MANE Select	NP_001361314.1:p.Phe567=
NM_001374386.1:c.1551T=	NP_001361315.1:p.Phe517=