Canonical Allele Identifier: CA2277808218

Gene: CCDC40

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80100342A= , CM000679.2:g.80100342A=	GRCh38
NC_000017.10:g.78074141A= , CM000679.1:g.78074141A=	GRCh37
NC_000017.9:g.75688736A=	NCBI36
NG_009822.1:g.3787A= , LRG_673:g.3787A=
NG_029761.1:g.68711A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397545.9:c.*567A= MANE Select	ENSP00000380679.4:n.*567A=
ENST00000397545.8:c.*567A=	ENSP00000380679.4:n.*567A=
ENST00000574799.5:n.3533A=
NM_017950.3:c.*567A=	NP_060420.2:n.*567A=
XM_011524963.1:c.*567A=	XP_011523265.1:n.*567A=
XM_011524964.1:c.*567A=	XP_011523266.1:n.*567A=
XM_011524963.3:c.*567A=	XP_011523265.1:n.*567A=
XM_011524964.3:c.*567A=	XP_011523266.1:n.*567A=
XM_024450821.1:c.*567A=	XP_024306589.1:n.*567A=
XR_934495.2:n.4114A=
NM_017950.4:c.*567A= MANE Select	NP_060420.2:n.*567A=