Canonical Allele Identifier: CA2229948856

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815636_68815637delinsAT , CM000678.2:g.68815636_68815637delinsAT	GRCh38
NC_000016.9:g.68849539_68849540delinsAT , CM000678.1:g.68849539_68849540delinsAT	GRCh37
NC_000016.8:g.67407040_67407041delinsAT	NCBI36
NG_008021.1:g.83345_83346delinsAT , LRG_301:g.83345_83346delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1442_1443delinsAT MANE Select	ENSP00000261769.4:p.Asn481=
ENST00000261769.9:c.1442_1443delinsAT	ENSP00000261769.4:p.Asn481=
ENST00000422392.6:c.1259_1260delinsAT	ENSP00000414946.2:p.Asn420=
ENST00000562836.5:n.1513_1514delinsAT
ENST00000566510.5:c.*108_*109delinsAT	ENSP00000458139.1:n.*108_*109delinsAT
ENST00000566612.5:c.1442_1443delinsAT	ENSP00000454782.1:p.Asn481=
ENST00000611625.4:c.1505_1506delinsAT	ENSP00000481063.1:p.Asn502=
ENST00000612417.4:c.1442_1443delinsAT	ENSP00000478360.1:p.Asn481=
ENST00000621016.4:c.1442_1443delinsAT	ENSP00000480664.1:p.Asn481=
NM_004360.3:c.1442_1443delinsAT , LRG_301t1:c.1442_1443delinsAT	NP_004351.1:p.Asn481=
XM_011523488.1:c.707_708delinsAT	XP_011521790.1:p.Asn236=
XM_011523489.1:c.707_708delinsAT	XP_011521791.1:p.Asn236=
NM_001317184.1:c.1259_1260delinsAT	NP_001304113.1:p.Asn420=
NM_001317185.1:c.-107_-106delinsAT	NP_001304114.1:n.-107_-106delinsAT
NM_001317186.1:c.-378_-377delinsAT	NP_001304115.1:n.-378_-377delinsAT
NM_004360.4:c.1442_1443delinsAT	NP_004351.1:p.Asn481=
NM_004360.5:c.1442_1443delinsAT MANE Select	NP_004351.1:p.Asn481=
NM_001317184.2:c.1259_1260delinsAT	NP_001304113.1:p.Asn420=
NM_001317185.2:c.-107_-106delinsAT	NP_001304114.1:n.-107_-106delinsAT
NM_001317186.2:c.-378_-377delinsAT	NP_001304115.1:n.-378_-377delinsAT