Canonical Allele Identifier: CA401351584

Gene: CCDC40

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80090181G>T , CM000679.2:g.80090181G>T	GRCh38
NC_000017.10:g.78063980G>T , CM000679.1:g.78063980G>T	GRCh37
NC_000017.9:g.75678575G>T	NCBI36
NG_029761.1:g.58550G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_017950.4:c.2832+297G>T MANE Select	NP_060420.2:n.2832+297G>T
ENST00000397545.9:c.2832+297G>T MANE Select	ENSP00000380679.4:n.2832+297G>T
NM_001243342.1:c.2875G>T	NP_001230271.1:p.Glu959Ter
NM_001243342.2:c.2875G>T	NP_001230271.1:p.Glu959Ter
NM_017950.3:c.2832+297G>T	NP_060420.2:n.2832+297G>T
ENST00000374877.7:c.2875G>T	ENSP00000364011.3:p.Glu959Ter
ENST00000397545.8:c.2832+297G>T	ENSP00000380679.4:n.2832+297G>T
ENST00000572253.5:n.3083+297G>T
ENST00000573903.1:n.494+297G>T
ENST00000574799.5:n.2369+297G>T
ENST00000575431.1:n.476+297G>T
XM_011524963.1:c.2742+297G>T	XP_011523265.1:n.2742+297G>T
XM_011524963.3:c.2742+297G>T	XP_011523265.1:n.2742+297G>T
XM_011524964.1:c.1653+297G>T	XP_011523266.1:n.1653+297G>T
XM_011524964.3:c.1653+297G>T	XP_011523266.1:n.1653+297G>T
XM_024450821.1:c.2742+297G>T	XP_024306589.1:n.2742+297G>T
XR_934495.2:n.2950+297G>T