Canonical Allele Identifier: CA408630150

Gene: SNTA1

Linked Data

• gnomAD v4: 20-33408740-A-T
• MyVariant Identifiers: chr20:g.31996546A>T (hg19) ; chr20:g.33408740A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33408740A>T , CM000682.2:g.33408740A>T	GRCh38
NC_000020.10:g.31996546A>T , CM000682.1:g.31996546A>T	GRCh37
NC_000020.9:g.31460207A>T	NCBI36
NG_011622.1:g.40153T>A , LRG_332:g.40153T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000217381.3:c.1386T>A MANE Select	ENSP00000217381.2:p.Ser462Arg
ENST00000217381.2:c.1386T>A	ENSP00000217381.2:p.Ser462Arg
NM_003098.2:c.1386T>A , LRG_332t1:c.1386T>A	NP_003089.1:p.Ser462Arg
XM_005260517.1:c.1386T>A	XP_005260574.1:p.Ser462Arg
XM_011529007.1:c.1418T>A	XP_011527309.1:p.Val473Asp
XM_011529008.1:c.1418T>A	XP_011527310.1:p.Val473Asp
XR_936612.1:n.1422T>A
XM_024451971.1:c.1059T>A	XP_024307739.1:p.Ser353Arg
NM_003098.3:c.1386T>A MANE Select	NP_003089.1:p.Ser462Arg