Canonical Allele Identifier: CA1452819068

Gene: ATP8A1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42410581C= , CM000666.2:g.42410581C=	GRCh38
NC_000004.11:g.42412598C= , CM000666.1:g.42412598C=	GRCh37
NC_000004.10:g.42107355C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000700470.1:c.*2335G=	ENSP00000515003.1:n.*2335G=
ENST00000264449.14:c.*2335G=	ENSP00000264449.10:n.*2335G=
ENST00000381668.9:c.*2335G= MANE Select	ENSP00000371084.5:n.*2335G=
ENST00000514372.5:c.3710G=	ENSP00000426495.1:n.3710G=
NM_001105529.1:c.*2335G=	NP_001098999.1:n.*2335G=
NM_006095.2:c.*2335G= MANE Select	NP_006086.1:n.*2335G=
XM_005248043.2:c.*2335G=	XP_005248100.1:n.*2335G=
XM_011513615.1:c.*2335G=	XP_011511917.1:n.*2335G=
XM_011513616.1:c.*2335G=	XP_011511918.1:n.*2335G=
XM_011513618.1:c.*2335G=	XP_011511920.1:n.*2335G=
XM_011513619.1:c.*2335G=	XP_011511921.1:n.*2335G=
XR_925118.1:n.5884G=
XM_005248043.3:c.*2335G=	XP_005248100.1:n.*2335G=
XM_011513615.2:c.*2335G=	XP_011511917.1:n.*2335G=
XM_011513616.3:c.*2335G=	XP_011511918.1:n.*2335G=
XM_011513618.2:c.*2335G=	XP_011511920.1:n.*2335G=
XM_017007645.2:c.*2335G=	XP_016863134.1:n.*2335G=
XM_017007646.1:c.*2335G=	XP_016863135.1:n.*2335G=
XM_017007647.1:c.*2335G=	XP_016863136.1:n.*2335G=
XR_001741094.2:n.5903G=
XR_925117.3:n.6097G=
XR_925118.2:n.5889G=
NM_001400024.1:c.*2335G=	NP_001386953.1:n.*2335G=
NM_001400025.1:c.*2335G=	NP_001386954.1:n.*2335G=
NM_001400026.1:c.*2335G=	NP_001386955.1:n.*2335G=
NM_001400027.1:c.*2335G=	NP_001386956.1:n.*2335G=