Canonical Allele Identifier: CA408424213
Gene: CST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23637701G>T , CM000682.2:g.23637701G>T GRCh38
NC_000020.10:g.23618338G>T , CM000682.1:g.23618338G>T GRCh37
NC_000020.9:g.23566338G>T NCBI36
NG_012887.2:g.5237C>A
NG_012887.3:g.5237C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376925.8:c.162C>A MANE Select ENSP00000366124.3:p.Asp54Glu
ENST00000376925.7:c.162C>A ENSP00000366124.3:p.Asp54Glu
ENST00000398409.1:c.162C>A ENSP00000381446.1:p.Asp54Glu
ENST00000398411.5:c.162C>A ENSP00000381448.1:p.Asp54Glu
NM_000099.3:c.162C>A NP_000090.1:p.Asp54Glu
NM_001288614.1:c.162C>A NP_001275543.1:p.Asp54Glu
NM_000099.4:c.162C>A MANE Select NP_000090.1:p.Asp54Glu
NM_001288614.2:c.162C>A NP_001275543.1:p.Asp54Glu