Canonical Allele Identifier: CA2640286704

Gene: CCDC40

Linked Data

• gnomAD v4: 17-80059123-T-TGGGGAGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80059123_80059124insGGGGAGGG , CM000679.2:g.80059123_80059124insGGGGAGGG	GRCh38
NC_000017.10:g.78032922_78032923insGGGGAGGG , CM000679.1:g.78032922_78032923insGGGGAGGG	GRCh37
NC_000017.9:g.75647517_75647518insGGGGAGGG	NCBI36
NG_029761.1:g.27492_27493insGGGGAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397545.9:c.1440+143_1440+144insGGGGAGGG MANE Select	ENSP00000380679.4:n.1440+143_1440+144insGGGGAGGG
ENST00000269318.9:c.1440+143_1440+144insGGGGAGGG	ENSP00000269318.5:n.1440+143_1440+144insGGGGAGGG
ENST00000374876.4:c.1317+472_1317+473insGGGGAGGG	ENSP00000364010.4:n.1317+472_1317+473insGGGGAGGG
ENST00000374877.7:c.1440+143_1440+144insGGGGAGGG	ENSP00000364011.3:n.1440+143_1440+144insGGGGAGGG
ENST00000397545.8:c.1440+143_1440+144insGGGGAGGG	ENSP00000380679.4:n.1440+143_1440+144insGGGGAGGG
ENST00000571028.1:c.56+143_56+144insGGGGAGGG
ENST00000574799.5:n.977+143_977+144insGGGGAGGG
NM_001243342.1:c.1440+143_1440+144insGGGGAGGG	NP_001230271.1:n.1440+143_1440+144insGGGGAGGG
NM_017950.3:c.1440+143_1440+144insGGGGAGGG	NP_060420.2:n.1440+143_1440+144insGGGGAGGG
XM_005257492.3:c.1440+143_1440+144insGGGGAGGG	XP_005257549.1:n.1440+143_1440+144insGGGGAGGG
XM_011524963.1:c.1350+143_1350+144insGGGGAGGG	XP_011523265.1:n.1350+143_1350+144insGGGGAGGG
XM_011524964.1:c.261+143_261+144insGGGGAGGG	XP_011523266.1:n.261+143_261+144insGGGGAGGG
XM_011524965.1:c.1440+143_1440+144insGGGGAGGG	XP_011523267.1:n.1440+143_1440+144insGGGGAGGG
XR_934495.1:n.1471+143_1471+144insGGGGAGGG
NM_001330508.1:c.1440+143_1440+144insGGGGAGGG	NP_001317437.1:n.1440+143_1440+144insGGGGAGGG
XM_011524963.3:c.1350+143_1350+144insGGGGAGGG	XP_011523265.1:n.1350+143_1350+144insGGGGAGGG
XM_011524964.3:c.261+143_261+144insGGGGAGGG	XP_011523266.1:n.261+143_261+144insGGGGAGGG
XM_011524965.3:c.1440+143_1440+144insGGGGAGGG	XP_011523267.1:n.1440+143_1440+144insGGGGAGGG
XM_017024807.1:c.1440+143_1440+144insGGGGAGGG	XP_016880296.1:n.1440+143_1440+144insGGGGAGGG
XM_024450821.1:c.1350+143_1350+144insGGGGAGGG	XP_024306589.1:n.1350+143_1350+144insGGGGAGGG
XR_001752550.2:n.1471+143_1471+144insGGGGAGGG
XR_934495.2:n.1471+143_1471+144insGGGGAGGG
NM_017950.4:c.1440+143_1440+144insGGGGAGGG MANE Select	NP_060420.2:n.1440+143_1440+144insGGGGAGGG
NM_001330508.2:c.1440+143_1440+144insGGGGAGGG	NP_001317437.1:n.1440+143_1440+144insGGGGAGGG
NM_001243342.2:c.1440+143_1440+144insGGGGAGGG	NP_001230271.1:n.1440+143_1440+144insGGGGAGGG