Canonical Allele Identifier: CA16616025
Gene: CCDC40 HGNC NCBI

Linked Data

dbSNP Id: rs1060501719
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80087748_80087749delinsACCG , CM000679.2:g.80087748_80087749delinsACCG GRCh38
NC_000017.10:g.78061547_78061548delinsACCG , CM000679.1:g.78061547_78061548delinsACCG GRCh37
NC_000017.9:g.75676142_75676143delinsACCG NCBI36
NG_029761.1:g.56117_56118delinsACCG

Transcript Alleles

HGVS Amino-acid change
ENST00000397545.9:c.2591_2592delinsACCG MANE Select ENSP00000380679.4:p.Thr864AsnfsTer10
ENST00000374877.7:c.2591_2592delinsACCG ENSP00000364011.3:p.Thr864AsnfsTer10
ENST00000397545.8:c.2591_2592delinsACCG ENSP00000380679.4:p.Thr864AsnfsTer10
ENST00000572253.5:n.2608_2609delinsACCG
ENST00000574799.5:n.2128_2129delinsACCG
ENST00000574933.1:n.46_47delinsACCG
ENST00000575431.1:n.235_236delinsACCG
NM_001243342.1:c.2591_2592delinsACCG NP_001230271.1:p.Thr864AsnfsTer10
NM_017950.3:c.2591_2592delinsACCG NP_060420.2:p.Thr864AsnfsTer10
XM_011524963.1:c.2501_2502delinsACCG XP_011523265.1:p.Thr834AsnfsTer10
XM_011524964.1:c.1412_1413delinsACCG XP_011523266.1:p.Thr471AsnfsTer10
XR_934495.1:n.2622_2623delinsACCG
XM_011524963.3:c.2501_2502delinsACCG XP_011523265.1:p.Thr834AsnfsTer10
XM_011524964.3:c.1412_1413delinsACCG XP_011523266.1:p.Thr471AsnfsTer10
XM_024450821.1:c.2501_2502delinsACCG XP_024306589.1:p.Thr834AsnfsTer10
XR_001752550.2:n.2622_2623delinsACCG
XR_934495.2:n.2622_2623delinsACCG
NM_017950.4:c.2591_2592delinsACCG MANE Select NP_060420.2:p.Thr864AsnfsTer10
NM_001243342.2:c.2591_2592delinsACCG NP_001230271.1:p.Thr864AsnfsTer10
Search 100 bp 5'
Search 100 bp 3'