Canonical Allele Identifier: CA408633596
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33438985A>C , CM000682.2:g.33438985A>C GRCh38
NC_000020.10:g.32026791A>C , CM000682.1:g.32026791A>C GRCh37
NC_000020.9:g.31490452A>C NCBI36
NG_011622.1:g.9908T>G , LRG_332:g.9908T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.352T>G MANE Select ENSP00000217381.2:p.Phe118Val
ENST00000217381.2:c.352T>G ENSP00000217381.2:p.Phe118Val
NM_003098.2:c.352T>G , LRG_332t1:c.352T>G NP_003089.1:p.Phe118Val
XM_005260517.1:c.352T>G XP_005260574.1:p.Phe118Val
XM_011529007.1:c.352T>G XP_011527309.1:p.Phe118Val
XM_011529008.1:c.352T>G XP_011527310.1:p.Phe118Val
XR_936612.1:n.585T>G
XM_024451971.1:c.25T>G XP_024307739.1:p.Phe9Val
NM_003098.3:c.352T>G MANE Select NP_003089.1:p.Phe118Val