Canonical Allele Identifier: CA1202192987
Gene: ATP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130511T= , CM000663.2:g.160130511T= GRCh38
NC_000001.10:g.160100301T= , CM000663.1:g.160100301T= GRCh37
NC_000001.9:g.158366925T= NCBI36
NG_008014.1:g.19754T= , LRG_6:g.19754T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.1741T= MANE Select ENSP00000354490.3:p.Cys581=
ENST00000361216.7:c.1741T= ENSP00000354490.3:p.Cys581=
ENST00000392233.7:c.1741T= ENSP00000376066.3:p.Cys581=
ENST00000447527.1:c.873T=
ENST00000472488.5:n.1844T=
NM_000702.3:c.1741T= NP_000693.1:p.Cys581=
NM_000702.4:c.1741T= MANE Select NP_000693.1:p.Cys581=
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Search 100 bp 3'