Canonical Allele Identifier: CA743727207

Gene: SNTA1

Linked Data

• dbSNP Id: rs1460572064
• MyVariant Identifiers: chr20:g.32026704del (hg19) ; chr20:g.33438898del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438898del , CM000682.2:g.33438898del	GRCh38
NC_000020.10:g.32026704del , CM000682.1:g.32026704del	GRCh37
NC_000020.9:g.31490365del	NCBI36
NG_011622.1:g.9995del , LRG_332:g.9995del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.439del MANE Select	ENSP00000217381.2:p.Thr147ProfsTer23
ENST00000217381.2:c.439del	ENSP00000217381.2:p.Thr147ProfsTer23
NM_003098.2:c.439del , LRG_332t1:c.439del	NP_003089.1:p.Thr147ProfsTer23
XM_005260517.1:c.439del	XP_005260574.1:p.Thr147ProfsTer23
XM_011529007.1:c.439del	XP_011527309.1:p.Thr147ProfsTer23
XM_011529008.1:c.439del	XP_011527310.1:p.Thr147ProfsTer23
XR_936612.1:n.672del
XM_024451971.1:c.112del	XP_024307739.1:p.Thr38ProfsTer23
NM_003098.3:c.439del MANE Select	NP_003089.1:p.Thr147ProfsTer23