Canonical Allele Identifier: CA408629900

Gene: SNTA1

Linked Data

• gnomAD v4: 20-33408529-G-T
• MyVariant Identifiers: chr20:g.31996335G>T (hg19) ; chr20:g.33408529G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33408529G>T , CM000682.2:g.33408529G>T	GRCh38
NC_000020.10:g.31996335G>T , CM000682.1:g.31996335G>T	GRCh37
NC_000020.9:g.31459996G>T	NCBI36
NG_011622.1:g.40364C>A , LRG_332:g.40364C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.1496C>A MANE Select	ENSP00000217381.2:p.Thr499Asn
ENST00000217381.2:c.1496C>A	ENSP00000217381.2:p.Thr499Asn
NM_003098.2:c.1496C>A , LRG_332t1:c.1496C>A	NP_003089.1:p.Thr499Asn
XM_005260517.1:c.1493C>A	XP_005260574.1:p.Thr498Asn
XM_011529007.1:c.*37C>A	XP_011527309.1:n.*37C>A
XM_011529008.1:c.*37C>A	XP_011527310.1:n.*37C>A
XR_936612.1:n.1532C>A
XM_024451971.1:c.1169C>A	XP_024307739.1:p.Thr390Asn
NM_003098.3:c.1496C>A MANE Select	NP_003089.1:p.Thr499Asn