Canonical Allele Identifier: CA343244326
Gene: ATP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130520G>A , CM000663.2:g.160130520G>A GRCh38
NC_000001.10:g.160100310G>A , CM000663.1:g.160100310G>A GRCh37
NC_000001.9:g.158366934G>A NCBI36
NG_008014.1:g.19763G>A , LRG_6:g.19763G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.1750G>A MANE Select ENSP00000354490.3:p.Gly584Arg
ENST00000361216.7:c.1750G>A ENSP00000354490.3:p.Gly584Arg
ENST00000392233.7:c.1750G>A ENSP00000376066.3:p.Gly584Arg
ENST00000447527.1:c.882G>A
ENST00000472488.5:n.1853G>A
NM_000702.3:c.1750G>A NP_000693.1:p.Gly584Arg
NM_000702.4:c.1750G>A MANE Select NP_000693.1:p.Gly584Arg