Canonical Allele Identifier: CA2360753149

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33439066C= , CM000682.2:g.33439066C=	GRCh38
NC_000020.10:g.32026872C= , CM000682.1:g.32026872C=	GRCh37
NC_000020.9:g.31490533C=	NCBI36
NG_011622.1:g.9827G= , LRG_332:g.9827G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.311-40G= MANE Select	ENSP00000217381.2:n.311-40G=
ENST00000217381.2:c.311-40G=	ENSP00000217381.2:n.311-40G=
NM_003098.2:c.311-40G= , LRG_332t1:c.311-40G=	NP_003089.1:n.311-40G=
XM_005260517.1:c.311-40G=	XP_005260574.1:n.311-40G=
XM_011529007.1:c.311-40G=	XP_011527309.1:n.311-40G=
XM_011529008.1:c.311-40G=	XP_011527310.1:n.311-40G=
XR_936612.1:n.544-40G=
XM_024451971.1:c.-17-40G=	XP_024307739.1:n.-17-40G=
NM_003098.3:c.311-40G= MANE Select	NP_003089.1:n.311-40G=