Canonical Allele Identifier: CA2277788112

Gene: CCDC40

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80058951_80058952delinsAC , CM000679.2:g.80058951_80058952delinsAC	GRCh38
NC_000017.10:g.78032750_78032751delinsAC , CM000679.1:g.78032750_78032751delinsAC	GRCh37
NC_000017.9:g.75647345_75647346delinsAC	NCBI36
NG_029761.1:g.27320_27321delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397545.9:c.1411_1412delinsAC MANE Select	ENSP00000380679.4:p.Thr471=
ENST00000269318.9:c.1411_1412delinsAC	ENSP00000269318.5:p.Thr471=
ENST00000374876.4:c.1317+300_1317+301delinsAC	ENSP00000364010.4:n.1317+300_1317+301delinsAC
ENST00000374877.7:c.1411_1412delinsAC	ENSP00000364011.3:p.Thr471=
ENST00000397545.8:c.1411_1412delinsAC	ENSP00000380679.4:p.Thr471=
ENST00000571028.1:c.27_28delinsAC
ENST00000574799.5:n.948_949delinsAC
NM_001243342.1:c.1411_1412delinsAC	NP_001230271.1:p.Thr471=
NM_017950.3:c.1411_1412delinsAC	NP_060420.2:p.Thr471=
XM_005257492.3:c.1411_1412delinsAC	XP_005257549.1:p.Thr471=
XM_011524963.1:c.1321_1322delinsAC	XP_011523265.1:p.Thr441=
XM_011524964.1:c.232_233delinsAC	XP_011523266.1:p.Thr78=
XM_011524965.1:c.1411_1412delinsAC	XP_011523267.1:p.Thr471=
XR_934495.1:n.1442_1443delinsAC
NM_001330508.1:c.1411_1412delinsAC	NP_001317437.1:p.Thr471=
XM_011524963.3:c.1321_1322delinsAC	XP_011523265.1:p.Thr441=
XM_011524964.3:c.232_233delinsAC	XP_011523266.1:p.Thr78=
XM_011524965.3:c.1411_1412delinsAC	XP_011523267.1:p.Thr471=
XM_017024807.1:c.1411_1412delinsAC	XP_016880296.1:p.Thr471=
XM_024450821.1:c.1321_1322delinsAC	XP_024306589.1:p.Thr441=
XR_001752550.2:n.1442_1443delinsAC
XR_934495.2:n.1442_1443delinsAC
NM_017950.4:c.1411_1412delinsAC MANE Select	NP_060420.2:p.Thr471=
NM_001330508.2:c.1411_1412delinsAC	NP_001317437.1:p.Thr471=
NM_001243342.2:c.1411_1412delinsAC	NP_001230271.1:p.Thr471=