Canonical Allele Identifier: CA401324579

Gene: CCDC40

Linked Data

• MyVariant Identifiers: chr17:g.78032742C>G (hg19) ; chr17:g.80058943C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80058943C>G , CM000679.2:g.80058943C>G	GRCh38
NC_000017.10:g.78032742C>G , CM000679.1:g.78032742C>G	GRCh37
NC_000017.9:g.75647337C>G	NCBI36
NG_029761.1:g.27312C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397545.9:c.1403C>G MANE Select	ENSP00000380679.4:p.Ala468Gly
ENST00000269318.9:c.1403C>G	ENSP00000269318.5:p.Ala468Gly
ENST00000374876.4:c.1317+292C>G	ENSP00000364010.4:n.1317+292C>G
ENST00000374877.7:c.1403C>G	ENSP00000364011.3:p.Ala468Gly
ENST00000397545.8:c.1403C>G	ENSP00000380679.4:p.Ala468Gly
ENST00000571028.1:c.19C>G
ENST00000574799.5:n.940C>G
NM_001243342.1:c.1403C>G	NP_001230271.1:p.Ala468Gly
NM_017950.3:c.1403C>G	NP_060420.2:p.Ala468Gly
XM_005257492.3:c.1403C>G	XP_005257549.1:p.Ala468Gly
XM_011524963.1:c.1313C>G	XP_011523265.1:p.Ala438Gly
XM_011524964.1:c.224C>G	XP_011523266.1:p.Ala75Gly
XM_011524965.1:c.1403C>G	XP_011523267.1:p.Ala468Gly
XR_934495.1:n.1434C>G
NM_001330508.1:c.1403C>G	NP_001317437.1:p.Ala468Gly
XM_011524963.3:c.1313C>G	XP_011523265.1:p.Ala438Gly
XM_011524964.3:c.224C>G	XP_011523266.1:p.Ala75Gly
XM_011524965.3:c.1403C>G	XP_011523267.1:p.Ala468Gly
XM_017024807.1:c.1403C>G	XP_016880296.1:p.Ala468Gly
XM_024450821.1:c.1313C>G	XP_024306589.1:p.Ala438Gly
XR_001752550.2:n.1434C>G
XR_934495.2:n.1434C>G
NM_017950.4:c.1403C>G MANE Select	NP_060420.2:p.Ala468Gly
NM_001330508.2:c.1403C>G	NP_001317437.1:p.Ala468Gly
NM_001243342.2:c.1403C>G	NP_001230271.1:p.Ala468Gly