Canonical Allele Identifier: CA2277808031

Gene: CCDC40

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80099924T= , CM000679.2:g.80099924T=	GRCh38
NC_000017.10:g.78073723T= , CM000679.1:g.78073723T=	GRCh37
NC_000017.9:g.75688318T=	NCBI36
NG_009822.1:g.3369T= , LRG_673:g.3369T=
NG_029761.1:g.68293T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397545.9:c.*149T= MANE Select	ENSP00000380679.4:n.*149T=
ENST00000397545.8:c.*149T=	ENSP00000380679.4:n.*149T=
ENST00000574799.5:n.3115T=
NM_017950.3:c.*149T=	NP_060420.2:n.*149T=
XM_011524963.1:c.*149T=	XP_011523265.1:n.*149T=
XM_011524964.1:c.*149T=	XP_011523266.1:n.*149T=
XM_011524963.3:c.*149T=	XP_011523265.1:n.*149T=
XM_011524964.3:c.*149T=	XP_011523266.1:n.*149T=
XM_024450821.1:c.*149T=	XP_024306589.1:n.*149T=
XR_934495.2:n.3696T=
NM_017950.4:c.*149T= MANE Select	NP_060420.2:n.*149T=