Canonical Allele Identifier: CA2652478421

Gene: SNTA1

Linked Data

• gnomAD v4: 20-33443593-TGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443597_33443598del , CM000682.2:g.33443597_33443598del	GRCh38
NC_000020.10:g.32031403_32031404del , CM000682.1:g.32031403_32031404del	GRCh37
NC_000020.9:g.31495064_31495065del	NCBI36
NG_011622.1:g.5298_5299del , LRG_332:g.5298_5299del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.26_27del MANE Select	ENSP00000217381.2:p.Arg9HisfsTer?
ENST00000217381.2:c.26_27del	ENSP00000217381.2:p.Arg9HisfsTer?
NM_003098.2:c.26_27del , LRG_332t1:c.26_27del	NP_003089.1:p.Arg9HisfsTer?
XM_005260517.1:c.26_27del	XP_005260574.1:p.Arg9HisfsTer?
XM_011529007.1:c.26_27del	XP_011527309.1:p.Arg9HisfsTer?
XM_011529008.1:c.26_27del	XP_011527310.1:p.Arg9HisfsTer?
XR_936612.1:n.259_260del
NM_003098.3:c.26_27del MANE Select	NP_003089.1:p.Arg9HisfsTer?