Canonical Allele Identifier: CA408633312
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33438852A>T , CM000682.2:g.33438852A>T GRCh38
NC_000020.10:g.32026658A>T , CM000682.1:g.32026658A>T GRCh37
NC_000020.9:g.31490319A>T NCBI36
NG_011622.1:g.10041T>A , LRG_332:g.10041T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.485T>A MANE Select ENSP00000217381.2:p.Val162Glu
ENST00000217381.2:c.485T>A ENSP00000217381.2:p.Val162Glu
NM_003098.2:c.485T>A , LRG_332t1:c.485T>A NP_003089.1:p.Val162Glu
XM_005260517.1:c.485T>A XP_005260574.1:p.Val162Glu
XM_011529007.1:c.485T>A XP_011527309.1:p.Val162Glu
XM_011529008.1:c.485T>A XP_011527310.1:p.Val162Glu
XR_936612.1:n.718T>A
XM_024451971.1:c.158T>A XP_024307739.1:p.Val53Glu
NM_003098.3:c.485T>A MANE Select NP_003089.1:p.Val162Glu