Canonical Allele Identifier: CA1202192876
Gene: ATP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130186T= , CM000663.2:g.160130186T= GRCh38
NC_000001.10:g.160099976T= , CM000663.1:g.160099976T= GRCh37
NC_000001.9:g.158366600T= NCBI36
NG_008014.1:g.19429T= , LRG_6:g.19429T=

Transcript Alleles

HGVS Amino-acid change
ENST00000361216.8:c.1546T= MANE Select ENSP00000354490.3:p.Ser516=
ENST00000361216.7:c.1546T= ENSP00000354490.3:p.Ser516=
ENST00000392233.7:c.1546T= ENSP00000376066.3:p.Ser516=
ENST00000447527.1:c.678T=
ENST00000472488.5:n.1649T=
NM_000702.3:c.1546T= NP_000693.1:p.Ser516=
NM_000702.4:c.1546T= MANE Select NP_000693.1:p.Ser516=