Canonical Allele Identifier: CA2360755026

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443597_33443598delinsCG , CM000682.2:g.33443597_33443598delinsCG	GRCh38
NC_000020.10:g.32031403_32031404delinsCG , CM000682.1:g.32031403_32031404delinsCG	GRCh37
NC_000020.9:g.31495064_31495065delinsCG	NCBI36
NG_011622.1:g.5295_5296delinsCG , LRG_332:g.5295_5296delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.23_24delinsCG MANE Select	ENSP00000217381.2:p.Pro8=
ENST00000217381.2:c.23_24delinsCG	ENSP00000217381.2:p.Pro8=
NM_003098.2:c.23_24delinsCG , LRG_332t1:c.23_24delinsCG	NP_003089.1:p.Pro8=
XM_005260517.1:c.23_24delinsCG	XP_005260574.1:p.Pro8=
XM_011529007.1:c.23_24delinsCG	XP_011527309.1:p.Pro8=
XM_011529008.1:c.23_24delinsCG	XP_011527310.1:p.Pro8=
XR_936612.1:n.256_257delinsCG
NM_003098.3:c.23_24delinsCG MANE Select	NP_003089.1:p.Pro8=