Canonical Allele Identifier: CA343237838
Gene: ATP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160127674C>G , CM000663.2:g.160127674C>G GRCh38
NC_000001.10:g.160097464C>G , CM000663.1:g.160097464C>G GRCh37
NC_000001.9:g.158364088C>G NCBI36
NG_008014.1:g.16917C>G , LRG_6:g.16917C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.871C>G MANE Select ENSP00000354490.3:p.Gln291Glu
ENST00000361216.7:c.871C>G ENSP00000354490.3:p.Gln291Glu
ENST00000392233.7:c.871C>G ENSP00000376066.3:p.Gln291Glu
ENST00000447527.1:c.3C>G
ENST00000472488.5:n.974C>G
NM_000702.3:c.871C>G NP_000693.1:p.Gln291Glu
NM_000702.4:c.871C>G MANE Select NP_000693.1:p.Gln291Glu