Canonical Allele Identifier: CA1202192967
Gene: ATP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130428G= , CM000663.2:g.160130428G= GRCh38
NC_000001.10:g.160100218G= , CM000663.1:g.160100218G= GRCh37
NC_000001.9:g.158366842G= NCBI36
NG_008014.1:g.19671G= , LRG_6:g.19671G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.1658G= MANE Select ENSP00000354490.3:p.Cys553=
ENST00000361216.7:c.1658G= ENSP00000354490.3:p.Cys553=
ENST00000392233.7:c.1658G= ENSP00000376066.3:p.Cys553=
ENST00000447527.1:c.790G=
ENST00000472488.5:n.1761G=
NM_000702.3:c.1658G= NP_000693.1:p.Cys553=
NM_000702.4:c.1658G= MANE Select NP_000693.1:p.Cys553=
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