Canonical Allele Identifier: CA401350745

Gene: CCDC40

Linked Data

• MyVariant Identifiers: chr17:g.78063562G>C (hg19) ; chr17:g.80089763G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80089763G>C , CM000679.2:g.80089763G>C	GRCh38
NC_000017.10:g.78063562G>C , CM000679.1:g.78063562G>C	GRCh37
NC_000017.9:g.75678157G>C	NCBI36
NG_029761.1:g.58132G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000397545.9:c.2712-1G>C MANE Select	ENSP00000380679.4:n.2712-1G>C
ENST00000374877.7:c.2712-1G>C	ENSP00000364011.3:n.2712-1G>C
ENST00000397545.8:c.2712-1G>C	ENSP00000380679.4:n.2712-1G>C
ENST00000572253.5:n.2963-1G>C
ENST00000573903.1:n.373G>C
ENST00000574799.5:n.2249-1G>C
ENST00000575431.1:n.356-1G>C
NM_001243342.1:c.2712-1G>C	NP_001230271.1:n.2712-1G>C
NM_017950.3:c.2712-1G>C	NP_060420.2:n.2712-1G>C
XM_011524963.1:c.2622-1G>C	XP_011523265.1:n.2622-1G>C
XM_011524964.1:c.1533-1G>C	XP_011523266.1:n.1533-1G>C
XR_934495.1:n.2830-1G>C
XM_011524963.3:c.2622-1G>C	XP_011523265.1:n.2622-1G>C
XM_011524964.3:c.1533-1G>C	XP_011523266.1:n.1533-1G>C
XM_024450821.1:c.2622-1G>C	XP_024306589.1:n.2622-1G>C
XR_934495.2:n.2830-1G>C
NM_017950.4:c.2712-1G>C MANE Select	NP_060420.2:n.2712-1G>C
NM_001243342.2:c.2712-1G>C	NP_001230271.1:n.2712-1G>C