Canonical Allele Identifier: CA2578985487

Gene: CDHR3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.106017927_106017928insCT , CM000669.2:g.106017927_106017928insCT	GRCh38
NC_000007.13:g.105658373_105658374insCT , CM000669.1:g.105658373_105658374insCT	GRCh37
NC_000007.12:g.105445609_105445610insCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317716.14:c.1508_1509insCT MANE Select	ENSP00000325954.9:p.Ala504TrpfsTer22
ENST00000317716.13:c.1508_1509insCT	ENSP00000325954.9:p.Ala504TrpfsTer22
ENST00000466045.1:c.700+1902_700+1903insCT	ENSP00000419017.1:n.700+1902_700+1903insCT
ENST00000468477.1:c.60-2446_60-2445insCT
ENST00000470188.5:n.1849+1902_1849+1903insCT
ENST00000478080.5:c.1244_1245insCT	ENSP00000417771.1:p.Ala416TrpfsTer22
NM_001301161.1:c.1244_1245insCT	NP_001288090.1:p.Ala416TrpfsTer22
NM_152750.4:c.1508_1509insCT	NP_689963.2:p.Ala504TrpfsTer22
XM_005250224.3:c.1244_1245insCT	XP_005250281.1:p.Ala416TrpfsTer22
XM_005250225.1:c.1508_1509insCT	XP_005250282.1:p.Ala504TrpfsTer22
XM_005250226.1:c.452_453insCT	XP_005250283.1:p.Ala152TrpfsTer22
XM_006715905.1:c.1426+1902_1426+1903insCT	XP_006715968.1:n.1426+1902_1426+1903insCT
XM_006715906.2:c.962_963insCT	XP_006715969.1:p.Ala322TrpfsTer22
XM_011515955.1:c.1508_1509insCT	XP_011514257.1:p.Ala504TrpfsTer22
XM_011515956.1:c.962_963insCT	XP_011514258.1:p.Ala322TrpfsTer22
XM_011515957.1:c.1508_1509insCT	XP_011514259.1:p.Ala504TrpfsTer22
XM_011515958.1:c.1426+1902_1426+1903insCT	XP_011514260.1:n.1426+1902_1426+1903insCT
XM_011515959.1:c.452_453insCT	XP_011514261.1:p.Ala152TrpfsTer22
XR_927414.1:n.1584_1585insCT
XM_005250224.5:c.1244_1245insCT	XP_005250281.1:p.Ala416TrpfsTer22
XM_005250225.2:c.1508_1509insCT	XP_005250282.1:p.Ala504TrpfsTer22
XM_006715905.2:c.1426+1902_1426+1903insCT	XP_006715968.1:n.1426+1902_1426+1903insCT
XM_011515955.2:c.1508_1509insCT	XP_011514257.1:p.Ala504TrpfsTer22
XM_011515956.2:c.962_963insCT	XP_011514258.1:p.Ala322TrpfsTer22
XM_011515957.2:c.1508_1509insCT	XP_011514259.1:p.Ala504TrpfsTer22
XM_011515958.2:c.1426+1902_1426+1903insCT	XP_011514260.1:n.1426+1902_1426+1903insCT
XM_011515959.2:c.452_453insCT	XP_011514261.1:p.Ala152TrpfsTer22
XM_017011862.1:c.1508_1509insCT	XP_016867351.1:p.Ala504TrpfsTer22
XM_017011863.2:c.962_963insCT	XP_016867352.1:p.Ala322TrpfsTer22
XM_017011864.1:c.962_963insCT	XP_016867353.1:p.Ala322TrpfsTer22
XM_017011865.2:c.1162+1902_1162+1903insCT	XP_016867354.1:n.1162+1902_1162+1903insCT
XM_017011866.2:c.659_660insCT	XP_016867355.1:p.Ala221TrpfsTer22
XM_017011867.2:c.880+1902_880+1903insCT	XP_016867356.1:n.880+1902_880+1903insCT
XM_024446689.1:c.452_453insCT	XP_024302457.1:p.Ala152TrpfsTer22
XM_024446690.1:c.577+1902_577+1903insCT	XP_024302458.1:n.577+1902_577+1903insCT
XR_001744598.1:n.1584_1585insCT
XR_001744600.2:n.1584_1585insCT
XR_001744601.2:n.1584_1585insCT
XR_001744602.1:n.1601_1602insCT
XR_001744603.2:n.1601_1602insCT
XR_001744604.2:n.1502+1902_1502+1903insCT
XR_001744605.2:n.1502+1902_1502+1903insCT
XR_001744606.2:n.1502+1902_1502+1903insCT
XR_001744607.2:n.1502+1902_1502+1903insCT
XR_927414.2:n.1584_1585insCT
NM_152750.5:c.1508_1509insCT MANE Select	NP_689963.2:p.Ala504TrpfsTer22
NM_001301161.2:c.1244_1245insCT	NP_001288090.1:p.Ala416TrpfsTer22