Canonical Allele Identifier: CA2652172010
Gene: CST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23637798_23637807del , CM000682.2:g.23637798_23637807del GRCh38
NC_000020.10:g.23618435_23618444del , CM000682.1:g.23618435_23618444del GRCh37
NC_000020.9:g.23566435_23566444del NCBI36
NG_012887.2:g.5131_5140del
NG_012887.3:g.5131_5140del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376925.8:c.56_65del MANE Select ENSP00000366124.3:p.Leu19ProfsTer14
ENST00000376925.7:c.56_65del ENSP00000366124.3:p.Leu19ProfsTer14
ENST00000398409.1:c.56_65del ENSP00000381446.1:p.Leu19ProfsTer14
ENST00000398411.5:c.56_65del ENSP00000381448.1:p.Leu19ProfsTer14
NM_000099.3:c.56_65del NP_000090.1:p.Leu19ProfsTer?
NM_001288614.1:c.56_65del NP_001275543.1:p.Leu19ProfsTer?
NM_000099.4:c.56_65del MANE Select NP_000090.1:p.Leu19ProfsTer14
NM_001288614.2:c.56_65del NP_001275543.1:p.Leu19ProfsTer14