Canonical Allele Identifier: CA2652171764
Gene: CST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23637691del , CM000682.2:g.23637691del GRCh38
NC_000020.10:g.23618328del , CM000682.1:g.23618328del GRCh37
NC_000020.9:g.23566328del NCBI36
NG_012887.2:g.5248del
NG_012887.3:g.5248del

Transcript Alleles

HGVS Amino-acid change
ENST00000376925.8:c.173del MANE Select ENSP00000366124.3:p.Gly58AlafsTer26
ENST00000376925.7:c.173del ENSP00000366124.3:p.Gly58AlafsTer26
ENST00000398409.1:c.173del ENSP00000381446.1:p.Gly58AlafsTer26
ENST00000398411.5:c.173del ENSP00000381448.1:p.Gly58AlafsTer26
NM_000099.3:c.173del NP_000090.1:p.Gly58AlafsTer26
NM_001288614.1:c.173del NP_001275543.1:p.Gly58AlafsTer26
NM_000099.4:c.173del MANE Select NP_000090.1:p.Gly58AlafsTer26
NM_001288614.2:c.173del NP_001275543.1:p.Gly58AlafsTer26