Canonical Allele Identifier: CA2810586106

Gene: CCDC40

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80099836A>C , CM000679.2:g.80099836A>C	GRCh38
NC_000017.10:g.78073635A>C , CM000679.1:g.78073635A>C	GRCh37
NC_000017.9:g.75688230A>C	NCBI36
NG_009822.1:g.3281A>C , LRG_673:g.3281A>C
NG_029761.1:g.68205A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397545.9:c.*61A>C MANE Select	ENSP00000380679.4:n.*61A>C
ENST00000397545.8:c.*61A>C	ENSP00000380679.4:n.*61A>C
ENST00000574799.5:n.3027A>C
NM_017950.3:c.*61A>C	NP_060420.2:n.*61A>C
XM_011524963.1:c.*61A>C	XP_011523265.1:n.*61A>C
XM_011524964.1:c.*61A>C	XP_011523266.1:n.*61A>C
XM_011524963.3:c.*61A>C	XP_011523265.1:n.*61A>C
XM_011524964.3:c.*61A>C	XP_011523266.1:n.*61A>C
XM_024450821.1:c.*61A>C	XP_024306589.1:n.*61A>C
XR_934495.2:n.3608A>C
NM_017950.4:c.*61A>C MANE Select	NP_060420.2:n.*61A>C