Canonical Allele Identifier: CA1142255462
Gene: ATP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160127567T= , CM000663.2:g.160127567T= GRCh38
NC_000001.10:g.160097357T= , CM000663.1:g.160097357T= GRCh37
NC_000001.9:g.158363981T= NCBI36
NG_008014.1:g.16810T= , LRG_6:g.16810T=

Transcript Alleles

HGVS Amino-acid change
ENST00000361216.8:c.764T= MANE Select ENSP00000354490.3:p.Ile255=
ENST00000361216.7:c.764T= ENSP00000354490.3:p.Ile255=
ENST00000392233.7:c.764T= ENSP00000376066.3:p.Ile255=
ENST00000472488.5:n.867T=
NM_000702.3:c.764T= NP_000693.1:p.Ile255=
NM_000702.4:c.764T= MANE Select NP_000693.1:p.Ile255=