Canonical Allele Identifier: CA2640267858
Gene: CCDC40 HGNC NCBI

Linked Data

gnomAD v4: 17-80099932-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80099932T>A , CM000679.2:g.80099932T>A GRCh38
NC_000017.10:g.78073731T>A , CM000679.1:g.78073731T>A GRCh37
NC_000017.9:g.75688326T>A NCBI36
NG_009822.1:g.3377T>A , LRG_673:g.3377T>A
NG_029761.1:g.68301T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000397545.9:c.*157T>A MANE Select ENSP00000380679.4:n.*157T>A
ENST00000397545.8:c.*157T>A ENSP00000380679.4:n.*157T>A
ENST00000574799.5:n.3123T>A
NM_017950.3:c.*157T>A NP_060420.2:n.*157T>A
XM_011524963.1:c.*157T>A XP_011523265.1:n.*157T>A
XM_011524964.1:c.*157T>A XP_011523266.1:n.*157T>A
XM_011524963.3:c.*157T>A XP_011523265.1:n.*157T>A
XM_011524964.3:c.*157T>A XP_011523266.1:n.*157T>A
XM_024450821.1:c.*157T>A XP_024306589.1:n.*157T>A
XR_934495.2:n.3704T>A
NM_017950.4:c.*157T>A MANE Select NP_060420.2:n.*157T>A
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