Canonical Allele Identifier: CA1149109322
Gene: ATP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130190C= , CM000663.2:g.160130190C= GRCh38
NC_000001.10:g.160099980C= , CM000663.1:g.160099980C= GRCh37
NC_000001.9:g.158366604C= NCBI36
NG_008014.1:g.19433C= , LRG_6:g.19433C=

Transcript Alleles

HGVS Amino-acid change
ENST00000361216.8:c.1550C= MANE Select ENSP00000354490.3:p.Thr517=
ENST00000361216.7:c.1550C= ENSP00000354490.3:p.Thr517=
ENST00000392233.7:c.1550C= ENSP00000376066.3:p.Thr517=
ENST00000447527.1:c.682C=
ENST00000472488.5:n.1653C=
NM_000702.3:c.1550C= NP_000693.1:p.Thr517=
NM_000702.4:c.1550C= MANE Select NP_000693.1:p.Thr517=