Canonical Allele Identifier: CA408634692
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443565G>C , CM000682.2:g.33443565G>C GRCh38
NC_000020.10:g.32031371G>C , CM000682.1:g.32031371G>C GRCh37
NC_000020.9:g.31495032G>C NCBI36
NG_011622.1:g.5328C>G , LRG_332:g.5328C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.56C>G MANE Select ENSP00000217381.2:p.Ala19Gly
ENST00000217381.2:c.56C>G ENSP00000217381.2:p.Ala19Gly
NM_003098.2:c.56C>G , LRG_332t1:c.56C>G NP_003089.1:p.Ala19Gly
XM_005260517.1:c.56C>G XP_005260574.1:p.Ala19Gly
XM_011529007.1:c.56C>G XP_011527309.1:p.Ala19Gly
XM_011529008.1:c.56C>G XP_011527310.1:p.Ala19Gly
XR_936612.1:n.289C>G
NM_003098.3:c.56C>G MANE Select NP_003089.1:p.Ala19Gly