Canonical Allele Identifier: CA2277800790

Gene: CCDC40

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80085794C= , CM000679.2:g.80085794C=	GRCh38
NC_000017.10:g.78059593C= , CM000679.1:g.78059593C=	GRCh37
NC_000017.9:g.75674188C=	NCBI36
NG_029761.1:g.54163C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000397545.9:c.2236-209C= MANE Select	ENSP00000380679.4:n.2236-209C=
ENST00000374877.7:c.2236-209C=	ENSP00000364011.3:n.2236-209C=
ENST00000397545.8:c.2236-209C=	ENSP00000380679.4:n.2236-209C=
ENST00000572253.5:n.863-209C=
ENST00000574799.5:n.1773-209C=
NM_001243342.1:c.2236-209C=	NP_001230271.1:n.2236-209C=
NM_017950.3:c.2236-209C=	NP_060420.2:n.2236-209C=
XM_011524963.1:c.2146-209C=	XP_011523265.1:n.2146-209C=
XM_011524964.1:c.1057-209C=	XP_011523266.1:n.1057-209C=
XR_934495.1:n.2267-209C=
XM_011524963.3:c.2146-209C=	XP_011523265.1:n.2146-209C=
XM_011524964.3:c.1057-209C=	XP_011523266.1:n.1057-209C=
XM_024450821.1:c.2146-209C=	XP_024306589.1:n.2146-209C=
XR_001752550.2:n.2267-209C=
XR_934495.2:n.2267-209C=
NM_017950.4:c.2236-209C= MANE Select	NP_060420.2:n.2236-209C=
NM_001243342.2:c.2236-209C=	NP_001230271.1:n.2236-209C=