Canonical Allele Identifier: CA1202191847

Gene: ATP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160127573T= , CM000663.2:g.160127573T=	GRCh38
NC_000001.10:g.160097363T= , CM000663.1:g.160097363T=	GRCh37
NC_000001.9:g.158363987T=	NCBI36
NG_008014.1:g.16816T= , LRG_6:g.16816T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000361216.8:c.770T= MANE Select	ENSP00000354490.3:p.Ile257=
ENST00000361216.7:c.770T=	ENSP00000354490.3:p.Ile257=
ENST00000392233.7:c.770T=	ENSP00000376066.3:p.Ile257=
ENST00000472488.5:n.873T=
NM_000702.3:c.770T=	NP_000693.1:p.Ile257=
NM_000702.4:c.770T= MANE Select	NP_000693.1:p.Ile257=