Canonical Allele Identifier: CA2355967103

Gene: CST3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23637708_23637717delinsGCACGCCGCA , CM000682.2:g.23637708_23637717delinsGCACGCCGCA	GRCh38
NC_000020.10:g.23618345_23618354delinsGCACGCCGCA , CM000682.1:g.23618345_23618354delinsGCACGCCGCA	GRCh37
NC_000020.9:g.23566345_23566354delinsGCACGCCGCA	NCBI36
NG_012887.2:g.5221_5230delinsTGCGGCGTGC
NG_012887.3:g.5221_5230delinsTGCGGCGTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376925.8:c.146_155delinsTGCGGCGTGC MANE Select	ENSP00000366124.3:p.Val49=
ENST00000376925.7:c.146_155delinsTGCGGCGTGC	ENSP00000366124.3:p.Val49=
ENST00000398409.1:c.146_155delinsTGCGGCGTGC	ENSP00000381446.1:p.Val49=
ENST00000398411.5:c.146_155delinsTGCGGCGTGC	ENSP00000381448.1:p.Val49=
NM_000099.3:c.146_155delinsTGCGGCGTGC	NP_000090.1:p.Val49=
NM_001288614.1:c.146_155delinsTGCGGCGTGC	NP_001275543.1:p.Val49=
NM_000099.4:c.146_155delinsTGCGGCGTGC MANE Select	NP_000090.1:p.Val49=
NM_001288614.2:c.146_155delinsTGCGGCGTGC	NP_001275543.1:p.Val49=