Canonical Allele Identifier: CA2761201015

Gene: ATP8A1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42410590C>A , CM000666.2:g.42410590C>A	GRCh38
NC_000004.11:g.42412607C>A , CM000666.1:g.42412607C>A	GRCh37
NC_000004.10:g.42107364C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000700470.1:c.*2326G>T	ENSP00000515003.1:n.*2326G>T
ENST00000264449.14:c.*2326G>T	ENSP00000264449.10:n.*2326G>T
ENST00000381668.9:c.*2326G>T MANE Select	ENSP00000371084.5:n.*2326G>T
ENST00000514372.5:c.3701G>T	ENSP00000426495.1:n.3701G>T
NM_001105529.1:c.*2326G>T	NP_001098999.1:n.*2326G>T
NM_006095.2:c.*2326G>T MANE Select	NP_006086.1:n.*2326G>T
XM_005248043.2:c.*2326G>T	XP_005248100.1:n.*2326G>T
XM_011513615.1:c.*2326G>T	XP_011511917.1:n.*2326G>T
XM_011513616.1:c.*2326G>T	XP_011511918.1:n.*2326G>T
XM_011513618.1:c.*2326G>T	XP_011511920.1:n.*2326G>T
XM_011513619.1:c.*2326G>T	XP_011511921.1:n.*2326G>T
XR_925118.1:n.5875G>T
XM_005248043.3:c.*2326G>T	XP_005248100.1:n.*2326G>T
XM_011513615.2:c.*2326G>T	XP_011511917.1:n.*2326G>T
XM_011513616.3:c.*2326G>T	XP_011511918.1:n.*2326G>T
XM_011513618.2:c.*2326G>T	XP_011511920.1:n.*2326G>T
XM_017007645.2:c.*2326G>T	XP_016863134.1:n.*2326G>T
XM_017007646.1:c.*2326G>T	XP_016863135.1:n.*2326G>T
XM_017007647.1:c.*2326G>T	XP_016863136.1:n.*2326G>T
XR_001741094.2:n.5894G>T
XR_925117.3:n.6088G>T
XR_925118.2:n.5880G>T
NM_001400024.1:c.*2326G>T	NP_001386953.1:n.*2326G>T
NM_001400025.1:c.*2326G>T	NP_001386954.1:n.*2326G>T
NM_001400026.1:c.*2326G>T	NP_001386955.1:n.*2326G>T
NM_001400027.1:c.*2326G>T	NP_001386956.1:n.*2326G>T