Canonical Allele Identifier: CA401324482
Gene: CCDC40 HGNC NCBI

Linked Data

dbSNP Id: rs2037823028

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80058900G>A , CM000679.2:g.80058900G>A GRCh38
NC_000017.10:g.78032699G>A , CM000679.1:g.78032699G>A GRCh37
NC_000017.9:g.75647294G>A NCBI36
NG_029761.1:g.27269G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000397545.9:c.1360G>A MANE Select ENSP00000380679.4:p.Glu454Lys
ENST00000269318.9:c.1360G>A ENSP00000269318.5:p.Glu454Lys
ENST00000374876.4:c.1317+249G>A ENSP00000364010.4:n.1317+249G>A
ENST00000374877.7:c.1360G>A ENSP00000364011.3:p.Glu454Lys
ENST00000397545.8:c.1360G>A ENSP00000380679.4:p.Glu454Lys
ENST00000574799.5:n.897G>A
NM_001243342.1:c.1360G>A NP_001230271.1:p.Glu454Lys
NM_017950.3:c.1360G>A NP_060420.2:p.Glu454Lys
XM_005257492.3:c.1360G>A XP_005257549.1:p.Glu454Lys
XM_011524963.1:c.1270G>A XP_011523265.1:p.Glu424Lys
XM_011524964.1:c.181G>A XP_011523266.1:p.Glu61Lys
XM_011524965.1:c.1360G>A XP_011523267.1:p.Glu454Lys
XR_934495.1:n.1391G>A
NM_001330508.1:c.1360G>A NP_001317437.1:p.Glu454Lys
XM_011524963.3:c.1270G>A XP_011523265.1:p.Glu424Lys
XM_011524964.3:c.181G>A XP_011523266.1:p.Glu61Lys
XM_011524965.3:c.1360G>A XP_011523267.1:p.Glu454Lys
XM_017024807.1:c.1360G>A XP_016880296.1:p.Glu454Lys
XM_024450821.1:c.1270G>A XP_024306589.1:p.Glu424Lys
XR_001752550.2:n.1391G>A
XR_934495.2:n.1391G>A
NM_017950.4:c.1360G>A MANE Select NP_060420.2:p.Glu454Lys
NM_001330508.2:c.1360G>A NP_001317437.1:p.Glu454Lys
NM_001243342.2:c.1360G>A NP_001230271.1:p.Glu454Lys