Canonical Allele Identifier: CA2576660580

Gene: CCDC40

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80099844C>G , CM000679.2:g.80099844C>G	GRCh38
NC_000017.10:g.78073643C>G , CM000679.1:g.78073643C>G	GRCh37
NC_000017.9:g.75688238C>G	NCBI36
NG_009822.1:g.3289C>G , LRG_673:g.3289C>G
NG_029761.1:g.68213C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397545.9:c.*69C>G MANE Select	ENSP00000380679.4:n.*69C>G
ENST00000397545.8:c.*69C>G	ENSP00000380679.4:n.*69C>G
ENST00000574799.5:n.3035C>G
NM_017950.3:c.*69C>G	NP_060420.2:n.*69C>G
XM_011524963.1:c.*69C>G	XP_011523265.1:n.*69C>G
XM_011524964.1:c.*69C>G	XP_011523266.1:n.*69C>G
XM_011524963.3:c.*69C>G	XP_011523265.1:n.*69C>G
XM_011524964.3:c.*69C>G	XP_011523266.1:n.*69C>G
XM_024450821.1:c.*69C>G	XP_024306589.1:n.*69C>G
XR_934495.2:n.3616C>G
NM_017950.4:c.*69C>G MANE Select	NP_060420.2:n.*69C>G