Canonical Allele Identifier: CA10651248

Gene: CCDC40

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80099961A>C , CM000679.2:g.80099961A>C	GRCh38
NC_000017.10:g.78073760A>C , CM000679.1:g.78073760A>C	GRCh37
NC_000017.9:g.75688355A>C	NCBI36
NG_009822.1:g.3406A>C , LRG_673:g.3406A>C
NG_029761.1:g.68330A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397545.9:c.*186A>C MANE Select	ENSP00000380679.4:n.*186A>C
ENST00000397545.8:c.*186A>C	ENSP00000380679.4:n.*186A>C
ENST00000574799.5:n.3152A>C
NM_017950.3:c.*186A>C	NP_060420.2:n.*186A>C
XM_011524963.1:c.*186A>C	XP_011523265.1:n.*186A>C
XM_011524964.1:c.*186A>C	XP_011523266.1:n.*186A>C
XM_011524963.3:c.*186A>C	XP_011523265.1:n.*186A>C
XM_011524964.3:c.*186A>C	XP_011523266.1:n.*186A>C
XM_024450821.1:c.*186A>C	XP_024306589.1:n.*186A>C
XR_934495.2:n.3733A>C
NM_017950.4:c.*186A>C MANE Select	NP_060420.2:n.*186A>C