Canonical Allele Identifier: CA2277804490

Gene: CCDC40

Linked Data

• dbSNP Id: rs2361701

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80092818G>C , CM000679.2:g.80092818G>C	GRCh38
NC_000017.10:g.78066617G>C , CM000679.1:g.78066617G>C	GRCh37
NC_000017.9:g.75681212G>C	NCBI36
NG_029761.1:g.61187G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000397545.9:c.2833-2445G>C MANE Select	ENSP00000380679.4:n.2833-2445G>C
ENST00000397545.8:c.2833-2445G>C	ENSP00000380679.4:n.2833-2445G>C
ENST00000572253.5:n.3084-2445G>C
ENST00000574799.5:n.2370-2445G>C
ENST00000575431.1:n.477-2445G>C
NM_017950.3:c.2833-2445G>C	NP_060420.2:n.2833-2445G>C
XM_011524963.1:c.2743-2445G>C	XP_011523265.1:n.2743-2445G>C
XM_011524964.1:c.1654-2445G>C	XP_011523266.1:n.1654-2445G>C
XM_011524963.3:c.2743-2445G>C	XP_011523265.1:n.2743-2445G>C
XM_011524964.3:c.1654-2445G>C	XP_011523266.1:n.1654-2445G>C
XM_024450821.1:c.2743-2445G>C	XP_024306589.1:n.2743-2445G>C
XR_934495.2:n.2951-2445G>C
NM_017950.4:c.2833-2445G>C MANE Select	NP_060420.2:n.2833-2445G>C