Canonical Allele Identifier: CA343244465
Gene: ATP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130563A>G , CM000663.2:g.160130563A>G GRCh38
NC_000001.10:g.160100353A>G , CM000663.1:g.160100353A>G GRCh37
NC_000001.9:g.158366977A>G NCBI36
NG_008014.1:g.19806A>G , LRG_6:g.19806A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.1793A>G MANE Select ENSP00000354490.3:p.Asp598Gly
ENST00000361216.7:c.1793A>G ENSP00000354490.3:p.Asp598Gly
ENST00000392233.7:c.1793A>G ENSP00000376066.3:p.Asp598Gly
ENST00000447527.1:c.925A>G
ENST00000472488.5:n.1896A>G
NM_000702.3:c.1793A>G NP_000693.1:p.Asp598Gly
NM_000702.4:c.1793A>G MANE Select NP_000693.1:p.Asp598Gly