Canonical Allele Identifier: CA1202191824
Gene: ATP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160127508_160127509delinsTG , CM000663.2:g.160127508_160127509delinsTG GRCh38
NC_000001.10:g.160097298_160097299delinsTG , CM000663.1:g.160097298_160097299delinsTG GRCh37
NC_000001.9:g.158363922_158363923delinsTG NCBI36
NG_008014.1:g.16751_16752delinsTG , LRG_6:g.16751_16752delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.749-44_749-43delinsTG MANE Select ENSP00000354490.3:n.749-44_749-43delinsTG
ENST00000361216.7:c.749-44_749-43delinsTG ENSP00000354490.3:n.749-44_749-43delinsTG
ENST00000392233.7:c.749-44_749-43delinsTG ENSP00000376066.3:n.749-44_749-43delinsTG
ENST00000472488.5:n.852-44_852-43delinsTG
NM_000702.3:c.749-44_749-43delinsTG NP_000693.1:n.749-44_749-43delinsTG
NM_000702.4:c.749-44_749-43delinsTG MANE Select NP_000693.1:n.749-44_749-43delinsTG