Canonical Allele Identifier: CA313275358

Gene: SNTA1

Linked Data

• dbSNP Id: rs949533969
• gnomAD v3: 20-33438520-AC-A
• gnomAD v4: 20-33438520-AC-A
• MyVariant Identifiers: chr20:g.32026327del (hg19) ; chr20:g.33438521del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438523del , CM000682.2:g.33438523del	GRCh38
NC_000020.10:g.32026329del , CM000682.1:g.32026329del	GRCh37
NC_000020.9:g.31489990del	NCBI36
NG_011622.1:g.10372del , LRG_332:g.10372del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+320del MANE Select	ENSP00000217381.2:n.496+320del
ENST00000217381.2:c.496+320del	ENSP00000217381.2:n.496+320del
NM_003098.2:c.496+320del , LRG_332t1:c.496+320del	NP_003089.1:n.496+320del
XM_005260517.1:c.496+320del	XP_005260574.1:n.496+320del
XM_011529007.1:c.496+320del	XP_011527309.1:n.496+320del
XM_011529008.1:c.496+320del	XP_011527310.1:n.496+320del
XR_936612.1:n.729+320del
XM_024451971.1:c.169+320del	XP_024307739.1:n.169+320del
NM_003098.3:c.496+320del MANE Select	NP_003089.1:n.496+320del