Canonical Allele Identifier: CA1202191804

Gene: ATP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160127466A= , CM000663.2:g.160127466A=	GRCh38
NC_000001.10:g.160097256A= , CM000663.1:g.160097256A=	GRCh37
NC_000001.9:g.158363880A=	NCBI36
NG_008014.1:g.16709A= , LRG_6:g.16709A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.749-86A= MANE Select	ENSP00000354490.3:n.749-86A=
ENST00000361216.7:c.749-86A=	ENSP00000354490.3:n.749-86A=
ENST00000392233.7:c.749-86A=	ENSP00000376066.3:n.749-86A=
ENST00000472488.5:n.852-86A=
NM_000702.3:c.749-86A=	NP_000693.1:n.749-86A=
NM_000702.4:c.749-86A= MANE Select	NP_000693.1:n.749-86A=