Canonical Allele Identifier: CA313279216

Gene: SNTA1

Linked Data

• dbSNP Id: rs891626566
• gnomAD v3: 20-33443693-C-CAGGGCAG
• gnomAD v4: 20-33443693-C-CAGGGCAG
• MyVariant Identifiers: chr20:g.32031499_32031500insAGGGCAG (hg19) ; chr20:g.33443693_33443694insAGGGCAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443701_33443707dup , CM000682.2:g.33443701_33443707dup	GRCh38
NC_000020.10:g.32031507_32031513dup , CM000682.1:g.32031507_32031513dup	GRCh37
NC_000020.9:g.31495168_31495174dup	NCBI36
NG_011622.1:g.5193_5199dup , LRG_332:g.5193_5199dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000217381.3:c.-80_-74dup MANE Select	ENSP00000217381.2:n.-80_-74dup
ENST00000217381.2:c.-80_-74dup	ENSP00000217381.2:n.-80_-74dup
NM_003098.2:c.-80_-74dup , LRG_332t1:c.-80_-74dup	NP_003089.1:n.-80_-74dup
XM_005260517.1:c.-80_-74dup	XP_005260574.1:n.-80_-74dup
XM_011529007.1:c.-80_-74dup	XP_011527309.1:n.-80_-74dup
XM_011529008.1:c.-80_-74dup	XP_011527310.1:n.-80_-74dup
XR_936612.1:n.154_160dup
NM_003098.3:c.-80_-74dup MANE Select	NP_003089.1:n.-80_-74dup