Canonical Allele Identifier: CA421599513

Gene: ATP1A2

Linked Data

• MyVariant Identifiers: chr1:g.160097400T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160127610T>A , CM000663.2:g.160127610T>A	GRCh38
NC_000001.10:g.160097400T>A , CM000663.1:g.160097400T>A	GRCh37
NC_000001.9:g.158364024T>A	NCBI36
NG_008014.1:g.16853T>A , LRG_6:g.16853T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.807T>A MANE Select	ENSP00000354490.3:p.Ala269=
ENST00000361216.7:c.807T>A	ENSP00000354490.3:p.Ala269=
ENST00000392233.7:c.807T>A	ENSP00000376066.3:p.Ala269=
ENST00000472488.5:n.910T>A
NM_000702.3:c.807T>A	NP_000693.1:p.Ala269=
NM_000702.4:c.807T>A MANE Select	NP_000693.1:p.Ala269=