Canonical Allele Identifier: CA2652478416

Gene: SNTA1

Linked Data

• gnomAD v4: 20-33443565-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443565_33443566insT , CM000682.2:g.33443565_33443566insT	GRCh38
NC_000020.10:g.32031371_32031372insT , CM000682.1:g.32031371_32031372insT	GRCh37
NC_000020.9:g.31495032_31495033insT	NCBI36
NG_011622.1:g.5327_5328insA , LRG_332:g.5327_5328insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.55_56insA MANE Select	ENSP00000217381.2:p.Ala19AspfsTer?
ENST00000217381.2:c.55_56insA	ENSP00000217381.2:p.Ala19AspfsTer?
NM_003098.2:c.55_56insA , LRG_332t1:c.55_56insA	NP_003089.1:p.Ala19AspfsTer?
XM_005260517.1:c.55_56insA	XP_005260574.1:p.Ala19AspfsTer?
XM_011529007.1:c.55_56insA	XP_011527309.1:p.Ala19AspfsTer?
XM_011529008.1:c.55_56insA	XP_011527310.1:p.Ala19AspfsTer?
XR_936612.1:n.288_289insA
NM_003098.3:c.55_56insA MANE Select	NP_003089.1:p.Ala19AspfsTer?