Canonical Allele Identifier: CA2576413763

Gene: CCDC40

Linked Data

• gnomAD v4: 17-80089693-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80089694dup , CM000679.2:g.80089694dup	GRCh38
NC_000017.10:g.78063493dup , CM000679.1:g.78063493dup	GRCh37
NC_000017.9:g.75678088dup	NCBI36
NG_029761.1:g.58063dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000397545.9:c.2712-70dup MANE Select	ENSP00000380679.4:n.2712-70dup
ENST00000374877.7:c.2712-70dup	ENSP00000364011.3:n.2712-70dup
ENST00000397545.8:c.2712-70dup	ENSP00000380679.4:n.2712-70dup
ENST00000572253.5:n.2963-70dup
ENST00000573903.1:n.304dup
ENST00000574799.5:n.2249-70dup
ENST00000575431.1:n.356-70dup
NM_001243342.1:c.2712-70dup	NP_001230271.1:n.2712-70dup
NM_017950.3:c.2712-70dup	NP_060420.2:n.2712-70dup
XM_011524963.1:c.2622-70dup	XP_011523265.1:n.2622-70dup
XM_011524964.1:c.1533-70dup	XP_011523266.1:n.1533-70dup
XR_934495.1:n.2830-70dup
XM_011524963.3:c.2622-70dup	XP_011523265.1:n.2622-70dup
XM_011524964.3:c.1533-70dup	XP_011523266.1:n.1533-70dup
XM_024450821.1:c.2622-70dup	XP_024306589.1:n.2622-70dup
XR_934495.2:n.2830-70dup
NM_017950.4:c.2712-70dup MANE Select	NP_060420.2:n.2712-70dup
NM_001243342.2:c.2712-70dup	NP_001230271.1:n.2712-70dup