Canonical Allele Identifier: CA2633932030

Gene: CDH1

Linked Data

• gnomAD v4: 16-68829890-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829891_68829892del , CM000678.2:g.68829891_68829892del	GRCh38
NC_000016.9:g.68863794_68863795del , CM000678.1:g.68863794_68863795del	GRCh37
NC_000016.8:g.67421295_67421296del	NCBI36
NG_008021.1:g.97600_97601del , LRG_301:g.97600_97601del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2439+94_2439+95del MANE Select	ENSP00000261769.4:n.2439+94_2439+95del
ENST00000261769.9:c.2439+94_2439+95del	ENSP00000261769.4:n.2439+94_2439+95del
ENST00000422392.6:c.2256+94_2256+95del	ENSP00000414946.2:n.2256+94_2256+95del
ENST00000562118.1:n.657+94_657+95del
ENST00000562836.5:n.2510+94_2510+95del
ENST00000566510.5:c.*1105+94_*1105+95del	ENSP00000458139.1:n.*1105+94_*1105+95del
ENST00000566612.5:c.*679+94_*679+95del	ENSP00000454782.1:n.*679+94_*679+95del
ENST00000611625.4:c.2502+94_2502+95del	ENSP00000481063.1:n.2502+94_2502+95del
ENST00000612417.4:c.1853+3337_1853+3338del	ENSP00000478360.1:n.1853+3337_1853+3338del
ENST00000621016.4:c.1866-4312_1866-4311del	ENSP00000480664.1:n.1866-4312_1866-4311del
NM_004360.3:c.2439+94_2439+95del , LRG_301t1:c.2439+94_2439+95del	NP_004351.1:n.2439+94_2439+95del
XM_011523488.1:c.1704+94_1704+95del	XP_011521790.1:n.1704+94_1704+95del
XM_011523489.1:c.1704+94_1704+95del	XP_011521791.1:n.1704+94_1704+95del
NM_001317184.1:c.2256+94_2256+95del	NP_001304113.1:n.2256+94_2256+95del
NM_001317185.1:c.891+94_891+95del	NP_001304114.1:n.891+94_891+95del
NM_001317186.1:c.474+94_474+95del	NP_001304115.1:n.474+94_474+95del
NM_004360.4:c.2439+94_2439+95del	NP_004351.1:n.2439+94_2439+95del
NM_004360.5:c.2439+94_2439+95del MANE Select	NP_004351.1:n.2439+94_2439+95del
NM_001317184.2:c.2256+94_2256+95del	NP_001304113.1:n.2256+94_2256+95del
NM_001317185.2:c.891+94_891+95del	NP_001304114.1:n.891+94_891+95del
NM_001317186.2:c.474+94_474+95del	NP_001304115.1:n.474+94_474+95del