Canonical Allele Identifier: CA408424193
Gene: CST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23637693A>C , CM000682.2:g.23637693A>C GRCh38
NC_000020.10:g.23618330A>C , CM000682.1:g.23618330A>C GRCh37
NC_000020.9:g.23566330A>C NCBI36
NG_012887.2:g.5245T>G
NG_012887.3:g.5245T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376925.8:c.170T>G MANE Select ENSP00000366124.3:p.Val57Gly
ENST00000376925.7:c.170T>G ENSP00000366124.3:p.Val57Gly
ENST00000398409.1:c.170T>G ENSP00000381446.1:p.Val57Gly
ENST00000398411.5:c.170T>G ENSP00000381448.1:p.Val57Gly
NM_000099.3:c.170T>G NP_000090.1:p.Val57Gly
NM_001288614.1:c.170T>G NP_001275543.1:p.Val57Gly
NM_000099.4:c.170T>G MANE Select NP_000090.1:p.Val57Gly
NM_001288614.2:c.170T>G NP_001275543.1:p.Val57Gly