Canonical Allele Identifier: CA2581725258
Gene: ATP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160127525C>G , CM000663.2:g.160127525C>G GRCh38
NC_000001.10:g.160097315C>G , CM000663.1:g.160097315C>G GRCh37
NC_000001.9:g.158363939C>G NCBI36
NG_008014.1:g.16768C>G , LRG_6:g.16768C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.749-27C>G MANE Select ENSP00000354490.3:n.749-27C>G
ENST00000361216.7:c.749-27C>G ENSP00000354490.3:n.749-27C>G
ENST00000392233.7:c.749-27C>G ENSP00000376066.3:n.749-27C>G
ENST00000472488.5:n.852-27C>G
NM_000702.3:c.749-27C>G NP_000693.1:n.749-27C>G
NM_000702.4:c.749-27C>G MANE Select NP_000693.1:n.749-27C>G