Canonical Allele Identifier: CA2695223622

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68819329_68819330del , CM000678.2:g.68819329_68819330del	GRCh38
NC_000016.9:g.68853232_68853233del , CM000678.1:g.68853232_68853233del	GRCh37
NC_000016.8:g.67410733_67410734del	NCBI36
NG_008021.1:g.87038_87039del , LRG_301:g.87038_87039del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1615_1616del MANE Select	ENSP00000261769.4:p.Thr539TrpfsTer8
ENST00000261769.9:c.1615_1616del	ENSP00000261769.4:p.Thr539TrpfsTer8
ENST00000422392.6:c.1432_1433del	ENSP00000414946.2:p.Thr478TrpfsTer8
ENST00000562836.5:n.1686_1687del
ENST00000566510.5:c.*281_*282del	ENSP00000458139.1:n.*281_*282del
ENST00000566612.5:c.1566-2672_1566-2671del	ENSP00000454782.1:n.1566-2672_1566-2671de...
ENST00000611625.4:c.1678_1679del	ENSP00000481063.1:p.Thr560TrpfsTer8
ENST00000612417.4:c.1615_1616del	ENSP00000478360.1:p.Thr539TrpfsTer8
ENST00000621016.4:c.1615_1616del	ENSP00000480664.1:p.Thr539TrpfsTer8
NM_004360.3:c.1615_1616del , LRG_301t1:c.1615_1616del	NP_004351.1:p.Thr539TrpfsTer8
XM_011523488.1:c.880_881del	XP_011521790.1:p.Thr294TrpfsTer8
XM_011523489.1:c.880_881del	XP_011521791.1:p.Thr294TrpfsTer8
NM_001317184.1:c.1432_1433del	NP_001304113.1:p.Thr478TrpfsTer8
NM_001317185.1:c.67_68del	NP_001304114.1:p.Thr23TrpfsTer8
NM_001317186.1:c.-254-2672_-254-2671del	NP_001304115.1:n.-254-2672_-254-2671del
NM_004360.4:c.1615_1616del	NP_004351.1:p.Thr539TrpfsTer8
NM_004360.5:c.1615_1616del MANE Select	NP_004351.1:p.Thr539TrpfsTer8
NM_001317184.2:c.1432_1433del	NP_001304113.1:p.Thr478TrpfsTer8
NM_001317185.2:c.67_68del	NP_001304114.1:p.Thr23TrpfsTer8
NM_001317186.2:c.-254-2672_-254-2671del	NP_001304115.1:n.-254-2672_-254-2671del