Canonical Allele Identifier: CA510163501

Gene: CST3

Linked Data

• gnomAD v4: 20-23637716-C-T
• MyVariant Identifiers: chr20:g.23618353C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23637716C>T , CM000682.2:g.23637716C>T	GRCh38
NC_000020.10:g.23618353C>T , CM000682.1:g.23618353C>T	GRCh37
NC_000020.9:g.23566353C>T	NCBI36
NG_012887.2:g.5222G>A
NG_012887.3:g.5222G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376925.8:c.147G>A MANE Select	ENSP00000366124.3:p.Val49=
ENST00000376925.7:c.147G>A	ENSP00000366124.3:p.Val49=
ENST00000398409.1:c.147G>A	ENSP00000381446.1:p.Val49=
ENST00000398411.5:c.147G>A	ENSP00000381448.1:p.Val49=
NM_000099.3:c.147G>A	NP_000090.1:p.Val49=
NM_001288614.1:c.147G>A	NP_001275543.1:p.Val49=
NM_000099.4:c.147G>A MANE Select	NP_000090.1:p.Val49=
NM_001288614.2:c.147G>A	NP_001275543.1:p.Val49=