Canonical Allele Identifier: CA343244223
Gene: ATP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130491A>C , CM000663.2:g.160130491A>C GRCh38
NC_000001.10:g.160100281A>C , CM000663.1:g.160100281A>C GRCh37
NC_000001.9:g.158366905A>C NCBI36
NG_008014.1:g.19734A>C , LRG_6:g.19734A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.1721A>C MANE Select ENSP00000354490.3:p.Asn574Thr
ENST00000361216.7:c.1721A>C ENSP00000354490.3:p.Asn574Thr
ENST00000392233.7:c.1721A>C ENSP00000376066.3:p.Asn574Thr
ENST00000447527.1:c.853A>C
ENST00000472488.5:n.1824A>C
NM_000702.3:c.1721A>C NP_000693.1:p.Asn574Thr
NM_000702.4:c.1721A>C MANE Select NP_000693.1:p.Asn574Thr