Canonical Allele Identifier: CA2277802642

Gene: CCDC40

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80089775T= , CM000679.2:g.80089775T=	GRCh38
NC_000017.10:g.78063574T= , CM000679.1:g.78063574T=	GRCh37
NC_000017.9:g.75678169T=	NCBI36
NG_029761.1:g.58144T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000397545.9:c.2723T= MANE Select	ENSP00000380679.4:p.Met908=
ENST00000374877.7:c.2723T=	ENSP00000364011.3:p.Met908=
ENST00000397545.8:c.2723T=	ENSP00000380679.4:p.Met908=
ENST00000572253.5:n.2974T=
ENST00000573903.1:n.385T=
ENST00000574799.5:n.2260T=
ENST00000575431.1:n.367T=
NM_001243342.1:c.2723T=	NP_001230271.1:p.Met908=
NM_017950.3:c.2723T=	NP_060420.2:p.Met908=
XM_011524963.1:c.2633T=	XP_011523265.1:p.Met878=
XM_011524964.1:c.1544T=	XP_011523266.1:p.Met515=
XR_934495.1:n.2841T=
XM_011524963.3:c.2633T=	XP_011523265.1:p.Met878=
XM_011524964.3:c.1544T=	XP_011523266.1:p.Met515=
XM_024450821.1:c.2633T=	XP_024306589.1:p.Met878=
XR_934495.2:n.2841T=
NM_017950.4:c.2723T= MANE Select	NP_060420.2:p.Met908=
NM_001243342.2:c.2723T=	NP_001230271.1:p.Met908=