Canonical Allele Identifier: CA10586037
Gene: ATP1A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 252573
ClinVar RCV Id: RCV000238744
dbSNP Id: rs879255368

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41984953C>T , CM000681.2:g.41984953C>T GRCh38
NC_000019.9:g.42489105C>T , CM000681.1:g.42489105C>T GRCh37
NC_000019.8:g.47180945C>T NCBI36
NG_008015.1:g.14278G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000545399.6:c.997G>A ENSP00000444688.1:p.Ala333Thr
ENST00000644613.1:c.958G>A ENSP00000494711.1:p.Ala320Thr
ENST00000648268.1:c.958G>A MANE Select ENSP00000498113.1:p.Ala320Thr
ENST00000302102.9:c.958G>A ENSP00000302397.5:p.Ala320Thr
ENST00000441343.5:c.958G>A ENSP00000411503.1:p.Ala320Thr
ENST00000485672.2:n.271G>A
ENST00000543770.5:c.991G>A ENSP00000437577.1:p.Ala331Thr
ENST00000545399.5:c.997G>A ENSP00000444688.1:p.Ala333Thr
ENST00000602133.5:c.868G>A ENSP00000471581.1:p.Ala290Thr
NM_001256213.1:c.991G>A NP_001243142.1:p.Ala331Thr
NM_001256214.1:c.997G>A NP_001243143.1:p.Ala333Thr
NM_152296.4:c.958G>A NP_689509.1:p.Ala320Thr
XM_011526991.1:c.868G>A XP_011525293.1:p.Ala290Thr
NM_152296.5:c.958G>A MANE Select NP_689509.1:p.Ala320Thr
NM_001256214.2:c.997G>A NP_001243143.1:p.Ala333Thr
NM_001256213.2:c.991G>A NP_001243142.1:p.Ala331Thr