Canonical Allele Identifier: CA1202196851

Gene: ATP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160139640G= , CM000663.2:g.160139640G=	GRCh38
NC_000001.10:g.160109430G= , CM000663.1:g.160109430G=	GRCh37
NC_000001.9:g.158376054G=	NCBI36
NG_008014.1:g.28883G= , LRG_6:g.28883G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.2841G= MANE Select	ENSP00000354490.3:p.Lys947=
ENST00000361216.7:c.2841G=	ENSP00000354490.3:p.Lys947=
ENST00000392233.7:c.2841G=	ENSP00000376066.3:p.Lys947=
ENST00000447527.1:c.1922G=
ENST00000463989.1:n.177G=
NM_000702.3:c.2841G=	NP_000693.1:p.Lys947=
NM_000702.4:c.2841G= MANE Select	NP_000693.1:p.Lys947=