Canonical Allele Identifier: CA1202192284

Gene: ATP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160128783C= , CM000663.2:g.160128783C=	GRCh38
NC_000001.10:g.160098573C= , CM000663.1:g.160098573C=	GRCh37
NC_000001.9:g.158365197C=	NCBI36
NG_008014.1:g.18026C= , LRG_6:g.18026C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000361216.8:c.1149C= MANE Select	ENSP00000354490.3:p.Arg383=
ENST00000361216.7:c.1149C=	ENSP00000354490.3:p.Arg383=
ENST00000392233.7:c.1149C=	ENSP00000376066.3:p.Arg383=
ENST00000447527.1:c.281C=
ENST00000472488.5:n.1252C=
NM_000702.3:c.1149C=	NP_000693.1:p.Arg383=
NM_000702.4:c.1149C= MANE Select	NP_000693.1:p.Arg383=