Canonical Allele Identifier: CA2815583551
Gene: CST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23637796_23637797dup , CM000682.2:g.23637796_23637797dup GRCh38
NC_000020.10:g.23618433_23618434dup , CM000682.1:g.23618433_23618434dup GRCh37
NC_000020.9:g.23566433_23566434dup NCBI36
NG_012887.2:g.5143_5144dup
NG_012887.3:g.5143_5144dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376925.8:c.68_69dup MANE Select ENSP00000366124.3:p.Ala24ProfsTer13
ENST00000376925.7:c.68_69dup ENSP00000366124.3:p.Ala24ProfsTer13
ENST00000398409.1:c.68_69dup ENSP00000381446.1:p.Ala24ProfsTer13
ENST00000398411.5:c.68_69dup ENSP00000381448.1:p.Ala24ProfsTer13
NM_000099.3:c.68_69dup NP_000090.1:p.Ala24ProfsTer?
NM_001288614.1:c.68_69dup NP_001275543.1:p.Ala24ProfsTer?
NM_000099.4:c.68_69dup MANE Select NP_000090.1:p.Ala24ProfsTer13
NM_001288614.2:c.68_69dup NP_001275543.1:p.Ala24ProfsTer13