Canonical Allele Identifier: CA1202192980

Gene: ATP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160130484G= , CM000663.2:g.160130484G=	GRCh38
NC_000001.10:g.160100274G= , CM000663.1:g.160100274G=	GRCh37
NC_000001.9:g.158366898G=	NCBI36
NG_008014.1:g.19727G= , LRG_6:g.19727G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.1714G= MANE Select	ENSP00000354490.3:p.Glu572=
ENST00000361216.7:c.1714G=	ENSP00000354490.3:p.Glu572=
ENST00000392233.7:c.1714G=	ENSP00000376066.3:p.Glu572=
ENST00000447527.1:c.846G=
ENST00000472488.5:n.1817G=
NM_000702.3:c.1714G=	NP_000693.1:p.Glu572=
NM_000702.4:c.1714G= MANE Select	NP_000693.1:p.Glu572=