Canonical Allele Identifier: CA313275425

Gene: SNTA1

Linked Data

• dbSNP Id: rs34260848

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438577dup , CM000682.2:g.33438577dup	GRCh38
NC_000020.10:g.32026383dup , CM000682.1:g.32026383dup	GRCh37
NC_000020.9:g.31490044dup	NCBI36
NG_011622.1:g.10318dup , LRG_332:g.10318dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+266dup MANE Select	ENSP00000217381.2:n.496+266dup
ENST00000217381.2:c.496+266dup	ENSP00000217381.2:n.496+266dup
NM_003098.2:c.496+266dup , LRG_332t1:c.496+266dup	NP_003089.1:n.496+266dup
XM_005260517.1:c.496+266dup	XP_005260574.1:n.496+266dup
XM_011529007.1:c.496+266dup	XP_011527309.1:n.496+266dup
XM_011529008.1:c.496+266dup	XP_011527310.1:n.496+266dup
XR_936612.1:n.729+266dup
XM_024451971.1:c.169+266dup	XP_024307739.1:n.169+266dup
NM_003098.3:c.496+266dup MANE Select	NP_003089.1:n.496+266dup