Canonical Allele Identifier: CA421599914
Gene: ATP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160098483C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160128693C>T , CM000663.2:g.160128693C>T GRCh38
NC_000001.10:g.160098483C>T , CM000663.1:g.160098483C>T GRCh37
NC_000001.9:g.158365107C>T NCBI36
NG_008014.1:g.17936C>T , LRG_6:g.17936C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.1059C>T MANE Select ENSP00000354490.3:p.Asn353=
ENST00000361216.7:c.1059C>T ENSP00000354490.3:p.Asn353=
ENST00000392233.7:c.1059C>T ENSP00000376066.3:p.Asn353=
ENST00000447527.1:c.191C>T
ENST00000472488.5:n.1162C>T
NM_000702.3:c.1059C>T NP_000693.1:p.Asn353=
NM_000702.4:c.1059C>T MANE Select NP_000693.1:p.Asn353=