Canonical Allele Identifier: CA2277788121

Gene: CCDC40

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80058970C= , CM000679.2:g.80058970C=	GRCh38
NC_000017.10:g.78032769C= , CM000679.1:g.78032769C=	GRCh37
NC_000017.9:g.75647364C=	NCBI36
NG_029761.1:g.27339C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397545.9:c.1430C= MANE Select	ENSP00000380679.4:p.Ala477=
ENST00000269318.9:c.1430C=	ENSP00000269318.5:p.Ala477=
ENST00000374876.4:c.1317+319C=	ENSP00000364010.4:n.1317+319C=
ENST00000374877.7:c.1430C=	ENSP00000364011.3:p.Ala477=
ENST00000397545.8:c.1430C=	ENSP00000380679.4:p.Ala477=
ENST00000571028.1:c.46C=
ENST00000574799.5:n.967C=
NM_001243342.1:c.1430C=	NP_001230271.1:p.Ala477=
NM_017950.3:c.1430C=	NP_060420.2:p.Ala477=
XM_005257492.3:c.1430C=	XP_005257549.1:p.Ala477=
XM_011524963.1:c.1340C=	XP_011523265.1:p.Ala447=
XM_011524964.1:c.251C=	XP_011523266.1:p.Ala84=
XM_011524965.1:c.1430C=	XP_011523267.1:p.Ala477=
XR_934495.1:n.1461C=
NM_001330508.1:c.1430C=	NP_001317437.1:p.Ala477=
XM_011524963.3:c.1340C=	XP_011523265.1:p.Ala447=
XM_011524964.3:c.251C=	XP_011523266.1:p.Ala84=
XM_011524965.3:c.1430C=	XP_011523267.1:p.Ala477=
XM_017024807.1:c.1430C=	XP_016880296.1:p.Ala477=
XM_024450821.1:c.1340C=	XP_024306589.1:p.Ala447=
XR_001752550.2:n.1461C=
XR_934495.2:n.1461C=
NM_017950.4:c.1430C= MANE Select	NP_060420.2:p.Ala477=
NM_001330508.2:c.1430C=	NP_001317437.1:p.Ala477=
NM_001243342.2:c.1430C=	NP_001230271.1:p.Ala477=