Canonical Allele Identifier: CA2540340762
Gene: ATP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160140013A>G , CM000663.2:g.160140013A>G GRCh38
NC_000001.10:g.160109803A>G , CM000663.1:g.160109803A>G GRCh37
NC_000001.9:g.158376427A>G NCBI36
NG_008014.1:g.29256A>G , LRG_6:g.29256A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.3034+29A>G MANE Select ENSP00000354490.3:n.3034+29A>G
ENST00000361216.7:c.3034+29A>G ENSP00000354490.3:n.3034+29A>G
ENST00000392233.7:c.3001+29A>G ENSP00000376066.3:n.3001+29A>G
ENST00000447527.1:c.2115+29A>G
ENST00000459972.1:n.26+29A>G
ENST00000463989.1:n.399A>G
NM_000702.3:c.3034+29A>G NP_000693.1:n.3034+29A>G
NM_000702.4:c.3034+29A>G MANE Select NP_000693.1:n.3034+29A>G