Canonical Allele Identifier: CA1202196952

Gene: ATP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160139956A= , CM000663.2:g.160139956A=	GRCh38
NC_000001.10:g.160109746A= , CM000663.1:g.160109746A=	GRCh37
NC_000001.9:g.158376370A=	NCBI36
NG_008014.1:g.29199A= , LRG_6:g.29199A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.3006A= MANE Select	ENSP00000354490.3:p.Arg1002=
ENST00000361216.7:c.3006A=	ENSP00000354490.3:p.Arg1002=
ENST00000392233.7:c.2973A=	ENSP00000376066.3:p.Arg991=
ENST00000447527.1:c.2087A=
ENST00000463989.1:n.342A=
NM_000702.3:c.3006A=	NP_000693.1:p.Arg1002=
NM_000702.4:c.3006A= MANE Select	NP_000693.1:p.Arg1002=