Canonical Allele Identifier: CA2277808033

Gene: CCDC40

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80099926G= , CM000679.2:g.80099926G=	GRCh38
NC_000017.10:g.78073725G= , CM000679.1:g.78073725G=	GRCh37
NC_000017.9:g.75688320G=	NCBI36
NG_009822.1:g.3371G= , LRG_673:g.3371G=
NG_029761.1:g.68295G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397545.9:c.*151G= MANE Select	ENSP00000380679.4:n.*151G=
ENST00000397545.8:c.*151G=	ENSP00000380679.4:n.*151G=
ENST00000574799.5:n.3117G=
NM_017950.3:c.*151G=	NP_060420.2:n.*151G=
XM_011524963.1:c.*151G=	XP_011523265.1:n.*151G=
XM_011524964.1:c.*151G=	XP_011523266.1:n.*151G=
XM_011524963.3:c.*151G=	XP_011523265.1:n.*151G=
XM_011524964.3:c.*151G=	XP_011523266.1:n.*151G=
XM_024450821.1:c.*151G=	XP_024306589.1:n.*151G=
XR_934495.2:n.3698G=
NM_017950.4:c.*151G= MANE Select	NP_060420.2:n.*151G=