Canonical Allele Identifier: CA408633497
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33438939T>G , CM000682.2:g.33438939T>G GRCh38
NC_000020.10:g.32026745T>G , CM000682.1:g.32026745T>G GRCh37
NC_000020.9:g.31490406T>G NCBI36
NG_011622.1:g.9954A>C , LRG_332:g.9954A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.398A>C MANE Select ENSP00000217381.2:p.Asp133Ala
ENST00000217381.2:c.398A>C ENSP00000217381.2:p.Asp133Ala
NM_003098.2:c.398A>C , LRG_332t1:c.398A>C NP_003089.1:p.Asp133Ala
XM_005260517.1:c.398A>C XP_005260574.1:p.Asp133Ala
XM_011529007.1:c.398A>C XP_011527309.1:p.Asp133Ala
XM_011529008.1:c.398A>C XP_011527310.1:p.Asp133Ala
XR_936612.1:n.631A>C
XM_024451971.1:c.71A>C XP_024307739.1:p.Asp24Ala
NM_003098.3:c.398A>C MANE Select NP_003089.1:p.Asp133Ala