Canonical Allele Identifier: CA1202191865

Gene: ATP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160127642C= , CM000663.2:g.160127642C=	GRCh38
NC_000001.10:g.160097432C= , CM000663.1:g.160097432C=	GRCh37
NC_000001.9:g.158364056C=	NCBI36
NG_008014.1:g.16885C= , LRG_6:g.16885C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.839C= MANE Select	ENSP00000354490.3:p.Thr280=
ENST00000361216.7:c.839C=	ENSP00000354490.3:p.Thr280=
ENST00000392233.7:c.839C=	ENSP00000376066.3:p.Thr280=
ENST00000472488.5:n.942C=
NM_000702.3:c.839C=	NP_000693.1:p.Thr280=
NM_000702.4:c.839C= MANE Select	NP_000693.1:p.Thr280=