Canonical Allele Identifier: CA645531311
Gene: ATP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160127636_160127637delinsAA , CM000663.2:g.160127636_160127637delinsAA GRCh38
NC_000001.10:g.160097426_160097427delinsAA , CM000663.1:g.160097426_160097427delinsAA GRCh37
NC_000001.9:g.158364050_158364051delinsAA NCBI36
NG_008014.1:g.16879_16880delinsAA , LRG_6:g.16879_16880delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.833_834delinsAA MANE Select ENSP00000354490.3:p.Gly278Glu
ENST00000361216.7:c.833_834delinsAA ENSP00000354490.3:p.Gly278Glu
ENST00000392233.7:c.833_834delinsAA ENSP00000376066.3:p.Gly278Glu
ENST00000472488.5:n.936_937delinsAA
NM_000702.3:c.833_834delinsAA NP_000693.1:p.Gly278Glu
NM_000702.4:c.833_834delinsAA MANE Select NP_000693.1:p.Gly278Glu