Canonical Allele Identifier: CA8813805
Gene: CCDC40 HGNC NCBI

Linked Data

dbSNP Id: rs761916536

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80058913C>T , CM000679.2:g.80058913C>T GRCh38
NC_000017.10:g.78032712C>T , CM000679.1:g.78032712C>T GRCh37
NC_000017.9:g.75647307C>T NCBI36
NG_029761.1:g.27282C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000397545.9:c.1373C>T MANE Select ENSP00000380679.4:p.Ala458Val
ENST00000269318.9:c.1373C>T ENSP00000269318.5:p.Ala458Val
ENST00000374876.4:c.1317+262C>T ENSP00000364010.4:n.1317+262C>T
ENST00000374877.7:c.1373C>T ENSP00000364011.3:p.Ala458Val
ENST00000397545.8:c.1373C>T ENSP00000380679.4:p.Ala458Val
ENST00000574799.5:n.910C>T
NM_001243342.1:c.1373C>T NP_001230271.1:p.Ala458Val
NM_017950.3:c.1373C>T NP_060420.2:p.Ala458Val
XM_005257492.3:c.1373C>T XP_005257549.1:p.Ala458Val
XM_011524963.1:c.1283C>T XP_011523265.1:p.Ala428Val
XM_011524964.1:c.194C>T XP_011523266.1:p.Ala65Val
XM_011524965.1:c.1373C>T XP_011523267.1:p.Ala458Val
XR_934495.1:n.1404C>T
NM_001330508.1:c.1373C>T NP_001317437.1:p.Ala458Val
XM_011524963.3:c.1283C>T XP_011523265.1:p.Ala428Val
XM_011524964.3:c.194C>T XP_011523266.1:p.Ala65Val
XM_011524965.3:c.1373C>T XP_011523267.1:p.Ala458Val
XM_017024807.1:c.1373C>T XP_016880296.1:p.Ala458Val
XM_024450821.1:c.1283C>T XP_024306589.1:p.Ala428Val
XR_001752550.2:n.1404C>T
XR_934495.2:n.1404C>T
NM_017950.4:c.1373C>T MANE Select NP_060420.2:p.Ala458Val
NM_001330508.2:c.1373C>T NP_001317437.1:p.Ala458Val
NM_001243342.2:c.1373C>T NP_001230271.1:p.Ala458Val