Canonical Allele Identifier: CA408424233

Gene: CST3

Linked Data

• gnomAD v4: 20-23637711-C-G
• MyVariant Identifiers: chr20:g.23618348C>G (hg19) ; chr20:g.23637711C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.23637711C>G , CM000682.2:g.23637711C>G	GRCh38
NC_000020.10:g.23618348C>G , CM000682.1:g.23618348C>G	GRCh37
NC_000020.9:g.23566348C>G	NCBI36
NG_012887.2:g.5227G>C
NG_012887.3:g.5227G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376925.8:c.152G>C MANE Select	ENSP00000366124.3:p.Arg51Pro
ENST00000376925.7:c.152G>C	ENSP00000366124.3:p.Arg51Pro
ENST00000398409.1:c.152G>C	ENSP00000381446.1:p.Arg51Pro
ENST00000398411.5:c.152G>C	ENSP00000381448.1:p.Arg51Pro
NM_000099.3:c.152G>C	NP_000090.1:p.Arg51Pro
NM_001288614.1:c.152G>C	NP_001275543.1:p.Arg51Pro
NM_000099.4:c.152G>C MANE Select	NP_000090.1:p.Arg51Pro
NM_001288614.2:c.152G>C	NP_001275543.1:p.Arg51Pro