Canonical Allele Identifier: CA2360752956

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438580A= , CM000682.2:g.33438580A=	GRCh38
NC_000020.10:g.32026386A= , CM000682.1:g.32026386A=	GRCh37
NC_000020.9:g.31490047A=	NCBI36
NG_011622.1:g.10313T= , LRG_332:g.10313T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+261T= MANE Select	ENSP00000217381.2:n.496+261T=
ENST00000217381.2:c.496+261T=	ENSP00000217381.2:n.496+261T=
NM_003098.2:c.496+261T= , LRG_332t1:c.496+261T=	NP_003089.1:n.496+261T=
XM_005260517.1:c.496+261T=	XP_005260574.1:n.496+261T=
XM_011529007.1:c.496+261T=	XP_011527309.1:n.496+261T=
XM_011529008.1:c.496+261T=	XP_011527310.1:n.496+261T=
XR_936612.1:n.729+261T=
XM_024451971.1:c.169+261T=	XP_024307739.1:n.169+261T=
NM_003098.3:c.496+261T= MANE Select	NP_003089.1:n.496+261T=