Canonical Allele Identifier: CA2640267856

Gene: CCDC40

Linked Data

• gnomAD v4: 17-80099931-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80099936del , CM000679.2:g.80099936del	GRCh38
NC_000017.10:g.78073735del , CM000679.1:g.78073735del	GRCh37
NC_000017.9:g.75688330del	NCBI36
NG_009822.1:g.3381del , LRG_673:g.3381del
NG_029761.1:g.68305del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397545.9:c.*161del MANE Select	ENSP00000380679.4:n.*161del
ENST00000397545.8:c.*161del	ENSP00000380679.4:n.*161del
ENST00000574799.5:n.3127del
NM_017950.3:c.*161del	NP_060420.2:n.*161del
XM_011524963.1:c.*161del	XP_011523265.1:n.*161del
XM_011524964.1:c.*161del	XP_011523266.1:n.*161del
XM_011524963.3:c.*161del	XP_011523265.1:n.*161del
XM_011524964.3:c.*161del	XP_011523266.1:n.*161del
XM_024450821.1:c.*161del	XP_024306589.1:n.*161del
XR_934495.2:n.3708del
NM_017950.4:c.*161del MANE Select	NP_060420.2:n.*161del