Canonical Allele Identifier: CA408634733

Gene: SNTA1

Linked Data

• gnomAD v4: 20-33443577-A-G
• MyVariant Identifiers: chr20:g.32031383A>G (hg19) ; chr20:g.33443577A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443577A>G , CM000682.2:g.33443577A>G	GRCh38
NC_000020.10:g.32031383A>G , CM000682.1:g.32031383A>G	GRCh37
NC_000020.9:g.31495044A>G	NCBI36
NG_011622.1:g.5316T>C , LRG_332:g.5316T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.44T>C MANE Select	ENSP00000217381.2:p.Leu15Pro
ENST00000217381.2:c.44T>C	ENSP00000217381.2:p.Leu15Pro
NM_003098.2:c.44T>C , LRG_332t1:c.44T>C	NP_003089.1:p.Leu15Pro
XM_005260517.1:c.44T>C	XP_005260574.1:p.Leu15Pro
XM_011529007.1:c.44T>C	XP_011527309.1:p.Leu15Pro
XM_011529008.1:c.44T>C	XP_011527310.1:p.Leu15Pro
XR_936612.1:n.277T>C
NM_003098.3:c.44T>C MANE Select	NP_003089.1:p.Leu15Pro