Canonical Allele Identifier: CA1202193006
Gene: ATP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130577T= , CM000663.2:g.160130577T= GRCh38
NC_000001.10:g.160100367T= , CM000663.1:g.160100367T= GRCh37
NC_000001.9:g.158366991T= NCBI36
NG_008014.1:g.19820T= , LRG_6:g.19820T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.1807T= MANE Select ENSP00000354490.3:p.Cys603=
ENST00000361216.7:c.1807T= ENSP00000354490.3:p.Cys603=
ENST00000392233.7:c.1807T= ENSP00000376066.3:p.Cys603=
ENST00000447527.1:c.939T=
ENST00000472488.5:n.1910T=
NM_000702.3:c.1807T= NP_000693.1:p.Cys603=
NM_000702.4:c.1807T= MANE Select NP_000693.1:p.Cys603=