Canonical Allele Identifier: CA2360755009

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443566_33443587delinsCCCCGGCGCGCAGCTCCAGCAG , CM000682.2:g.33443566_33443587delinsCCCCGGCGCGCAGCTCCAGCAG	GRCh38
NC_000020.10:g.32031372_32031393delinsCCCCGGCGCGCAGCTCCAGCAG , CM000682.1:g.32031372_32031393delinsCCCCGGCGCGCAGCTCCAGCAG	GRCh37
NC_000020.9:g.31495033_31495054delinsCCCCGGCGCGCAGCTCCAGCAG	NCBI36
NG_011622.1:g.5306_5327delinsCTGCTGGAGCTGCGCGCCGGGG , LRG_332:g.5306_5327delinsCTGCTGGAGCTGCGCGCCGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.34_55delinsCTGCTGGAGCTGCGCGCCGGGG MANE Select	ENSP00000217381.2:p.Leu12=
ENST00000217381.2:c.34_55delinsCTGCTGGAGCTGCGCGCCGGGG	ENSP00000217381.2:p.Leu12=
NM_003098.2:c.34_55delinsCTGCTGGAGCTGCGCGCCGGGG , LRG_332t1:c.34_55delinsCTGCTGGAGCTGCGCGCCGGGG	NP_003089.1:p.Leu12=
XM_005260517.1:c.34_55delinsCTGCTGGAGCTGCGCGCCGGGG	XP_005260574.1:p.Leu12=
XM_011529007.1:c.34_55delinsCTGCTGGAGCTGCGCGCCGGGG	XP_011527309.1:p.Leu12=
XM_011529008.1:c.34_55delinsCTGCTGGAGCTGCGCGCCGGGG	XP_011527310.1:p.Leu12=
XR_936612.1:n.267_288delinsCTGCTGGAGCTGCGCGCCGGGG
NM_003098.3:c.34_55delinsCTGCTGGAGCTGCGCGCCGGGG MANE Select	NP_003089.1:p.Leu12=