Canonical Allele Identifier: CA408633610
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1466316930

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33438990T>G , CM000682.2:g.33438990T>G GRCh38
NC_000020.10:g.32026796T>G , CM000682.1:g.32026796T>G GRCh37
NC_000020.9:g.31490457T>G NCBI36
NG_011622.1:g.9903A>C , LRG_332:g.9903A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.347A>C MANE Select ENSP00000217381.2:p.Lys116Thr
ENST00000217381.2:c.347A>C ENSP00000217381.2:p.Lys116Thr
NM_003098.2:c.347A>C , LRG_332t1:c.347A>C NP_003089.1:p.Lys116Thr
XM_005260517.1:c.347A>C XP_005260574.1:p.Lys116Thr
XM_011529007.1:c.347A>C XP_011527309.1:p.Lys116Thr
XM_011529008.1:c.347A>C XP_011527310.1:p.Lys116Thr
XR_936612.1:n.580A>C
XM_024451971.1:c.20A>C XP_024307739.1:p.Lys7Thr
NM_003098.3:c.347A>C MANE Select NP_003089.1:p.Lys116Thr