Canonical Allele Identifier: CA1202191812

Gene: ATP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160127484G= , CM000663.2:g.160127484G=	GRCh38
NC_000001.10:g.160097274G= , CM000663.1:g.160097274G=	GRCh37
NC_000001.9:g.158363898G=	NCBI36
NG_008014.1:g.16727G= , LRG_6:g.16727G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.749-68G= MANE Select	ENSP00000354490.3:n.749-68G=
ENST00000361216.7:c.749-68G=	ENSP00000354490.3:n.749-68G=
ENST00000392233.7:c.749-68G=	ENSP00000376066.3:n.749-68G=
ENST00000472488.5:n.852-68G=
NM_000702.3:c.749-68G=	NP_000693.1:n.749-68G=
NM_000702.4:c.749-68G= MANE Select	NP_000693.1:n.749-68G=