Canonical Allele Identifier: CA2360752999

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438680C= , CM000682.2:g.33438680C=	GRCh38
NC_000020.10:g.32026486C= , CM000682.1:g.32026486C=	GRCh37
NC_000020.9:g.31490147C=	NCBI36
NG_011622.1:g.10213G= , LRG_332:g.10213G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+161G= MANE Select	ENSP00000217381.2:n.496+161G=
ENST00000217381.2:c.496+161G=	ENSP00000217381.2:n.496+161G=
NM_003098.2:c.496+161G= , LRG_332t1:c.496+161G=	NP_003089.1:n.496+161G=
XM_005260517.1:c.496+161G=	XP_005260574.1:n.496+161G=
XM_011529007.1:c.496+161G=	XP_011527309.1:n.496+161G=
XM_011529008.1:c.496+161G=	XP_011527310.1:n.496+161G=
XR_936612.1:n.729+161G=
XM_024451971.1:c.169+161G=	XP_024307739.1:n.169+161G=
NM_003098.3:c.496+161G= MANE Select	NP_003089.1:n.496+161G=