Canonical Allele Identifier: CA510163489

Gene: CST3

Linked Data

• gnomAD v4: 20-23637707-T-A
• MyVariant Identifiers: chr20:g.23618344T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23637707T>A , CM000682.2:g.23637707T>A	GRCh38
NC_000020.10:g.23618344T>A , CM000682.1:g.23618344T>A	GRCh37
NC_000020.9:g.23566344T>A	NCBI36
NG_012887.2:g.5231A>T
NG_012887.3:g.5231A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376925.8:c.156A>T MANE Select	ENSP00000366124.3:p.Ala52=
ENST00000376925.7:c.156A>T	ENSP00000366124.3:p.Ala52=
ENST00000398409.1:c.156A>T	ENSP00000381446.1:p.Ala52=
ENST00000398411.5:c.156A>T	ENSP00000381448.1:p.Ala52=
NM_000099.3:c.156A>T	NP_000090.1:p.Ala52=
NM_001288614.1:c.156A>T	NP_001275543.1:p.Ala52=
NM_000099.4:c.156A>T MANE Select	NP_000090.1:p.Ala52=
NM_001288614.2:c.156A>T	NP_001275543.1:p.Ala52=