Canonical Allele Identifier: CA2360755109

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443716C= , CM000682.2:g.33443716C=	GRCh38
NC_000020.10:g.32031522C= , CM000682.1:g.32031522C=	GRCh37
NC_000020.9:g.31495183C=	NCBI36
NG_011622.1:g.5177G= , LRG_332:g.5177G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.-96G= MANE Select	ENSP00000217381.2:n.-96G=
ENST00000217381.2:c.-96G=	ENSP00000217381.2:n.-96G=
NM_003098.2:c.-96G= , LRG_332t1:c.-96G=	NP_003089.1:n.-96G=
XM_005260517.1:c.-96G=	XP_005260574.1:n.-96G=
XM_011529007.1:c.-96G=	XP_011527309.1:n.-96G=
XM_011529008.1:c.-96G=	XP_011527310.1:n.-96G=
XR_936612.1:n.138G=
NM_003098.3:c.-96G= MANE Select	NP_003089.1:n.-96G=