Canonical Allele Identifier: CA986705543

Gene: CCDC40

Linked Data

• gnomAD v3: 17-80085822-A-ATG
• gnomAD v4: 17-80085822-A-ATG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80085822_80085823insTG , CM000679.2:g.80085822_80085823insTG	GRCh38
NC_000017.10:g.78059621_78059622insTG , CM000679.1:g.78059621_78059622insTG	GRCh37
NC_000017.9:g.75674216_75674217insTG	NCBI36
NG_029761.1:g.54191_54192insTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000397545.9:c.2236-181_2236-180insTG MANE Select	ENSP00000380679.4:n.2236-181_2236-180insTG
ENST00000374877.7:c.2236-181_2236-180insTG	ENSP00000364011.3:n.2236-181_2236-180insTG
ENST00000397545.8:c.2236-181_2236-180insTG	ENSP00000380679.4:n.2236-181_2236-180insTG
ENST00000572253.5:n.863-181_863-180insTG
ENST00000574799.5:n.1773-181_1773-180insTG
NM_001243342.1:c.2236-181_2236-180insTG	NP_001230271.1:n.2236-181_2236-180insTG
NM_017950.3:c.2236-181_2236-180insTG	NP_060420.2:n.2236-181_2236-180insTG
XM_011524963.1:c.2146-181_2146-180insTG	XP_011523265.1:n.2146-181_2146-180insTG
XM_011524964.1:c.1057-181_1057-180insTG	XP_011523266.1:n.1057-181_1057-180insTG
XR_934495.1:n.2267-181_2267-180insTG
XM_011524963.3:c.2146-181_2146-180insTG	XP_011523265.1:n.2146-181_2146-180insTG
XM_011524964.3:c.1057-181_1057-180insTG	XP_011523266.1:n.1057-181_1057-180insTG
XM_024450821.1:c.2146-181_2146-180insTG	XP_024306589.1:n.2146-181_2146-180insTG
XR_001752550.2:n.2267-181_2267-180insTG
XR_934495.2:n.2267-181_2267-180insTG
NM_017950.4:c.2236-181_2236-180insTG MANE Select	NP_060420.2:n.2236-181_2236-180insTG
NM_001243342.2:c.2236-181_2236-180insTG	NP_001230271.1:n.2236-181_2236-180insTG