Canonical Allele Identifier: CA408424211
Gene: CST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23637700A>T , CM000682.2:g.23637700A>T GRCh38
NC_000020.10:g.23618337A>T , CM000682.1:g.23618337A>T GRCh37
NC_000020.9:g.23566337A>T NCBI36
NG_012887.2:g.5238T>A
NG_012887.3:g.5238T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376925.8:c.163T>A MANE Select ENSP00000366124.3:p.Phe55Ile
ENST00000376925.7:c.163T>A ENSP00000366124.3:p.Phe55Ile
ENST00000398409.1:c.163T>A ENSP00000381446.1:p.Phe55Ile
ENST00000398411.5:c.163T>A ENSP00000381448.1:p.Phe55Ile
NM_000099.3:c.163T>A NP_000090.1:p.Phe55Ile
NM_001288614.1:c.163T>A NP_001275543.1:p.Phe55Ile
NM_000099.4:c.163T>A MANE Select NP_000090.1:p.Phe55Ile
NM_001288614.2:c.163T>A NP_001275543.1:p.Phe55Ile