Canonical Allele Identifier: CA2229978070
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819347_68819348delinsCG , CM000678.2:g.68819347_68819348delinsCG GRCh38
NC_000016.9:g.68853250_68853251delinsCG , CM000678.1:g.68853250_68853251delinsCG GRCh37
NC_000016.8:g.67410751_67410752delinsCG NCBI36
NG_008021.1:g.87056_87057delinsCG , LRG_301:g.87056_87057delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1633_1634delinsCG MANE Select ENSP00000261769.4:p.Arg545=
ENST00000261769.9:c.1633_1634delinsCG ENSP00000261769.4:p.Arg545=
ENST00000422392.6:c.1450_1451delinsCG ENSP00000414946.2:p.Arg484=
ENST00000562836.5:n.1704_1705delinsCG
ENST00000566510.5:c.*299_*300delinsCG ENSP00000458139.1:n.*299_*300delinsCG
ENST00000566612.5:c.1566-2654_1566-2653delinsCG ENSP00000454782.1:n.1566-2654_1566-2653delinsCG
ENST00000611625.4:c.1696_1697delinsCG ENSP00000481063.1:p.Arg566=
ENST00000612417.4:c.1633_1634delinsCG ENSP00000478360.1:p.Arg545=
ENST00000621016.4:c.1633_1634delinsCG ENSP00000480664.1:p.Arg545=
NM_004360.3:c.1633_1634delinsCG , LRG_301t1:c.1633_1634delinsCG NP_004351.1:p.Arg545=
XM_011523488.1:c.898_899delinsCG XP_011521790.1:p.Arg300=
XM_011523489.1:c.898_899delinsCG XP_011521791.1:p.Arg300=
NM_001317184.1:c.1450_1451delinsCG NP_001304113.1:p.Arg484=
NM_001317185.1:c.85_86delinsCG NP_001304114.1:p.Arg29=
NM_001317186.1:c.-254-2654_-254-2653delinsCG NP_001304115.1:n.-254-2654_-254-2653delinsCG
NM_004360.4:c.1633_1634delinsCG NP_004351.1:p.Arg545=
NM_004360.5:c.1633_1634delinsCG MANE Select NP_004351.1:p.Arg545=
NM_001317184.2:c.1450_1451delinsCG NP_001304113.1:p.Arg484=
NM_001317185.2:c.85_86delinsCG NP_001304114.1:p.Arg29=
NM_001317186.2:c.-254-2654_-254-2653delinsCG NP_001304115.1:n.-254-2654_-254-2653delinsCG