Canonical Allele Identifier: CA2581284979

Gene: CCDC40

Genomic Alleles

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

Transcript Alleles

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