Canonical Allele Identifier: CA2633932026

Gene: CDH1

Linked Data

• gnomAD v4: 16-68829887-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829889_68829890dup , CM000678.2:g.68829889_68829890dup	GRCh38
NC_000016.9:g.68863792_68863793dup , CM000678.1:g.68863792_68863793dup	GRCh37
NC_000016.8:g.67421293_67421294dup	NCBI36
NG_008021.1:g.97598_97599dup , LRG_301:g.97598_97599dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2439+92_2439+93dup MANE Select	ENSP00000261769.4:n.2439+92_2439+93dup
ENST00000261769.9:c.2439+92_2439+93dup	ENSP00000261769.4:n.2439+92_2439+93dup
ENST00000422392.6:c.2256+92_2256+93dup	ENSP00000414946.2:n.2256+92_2256+93dup
ENST00000562118.1:n.657+92_657+93dup
ENST00000562836.5:n.2510+92_2510+93dup
ENST00000566510.5:c.*1105+92_*1105+93dup	ENSP00000458139.1:n.*1105+92_*1105+93dup
ENST00000566612.5:c.*679+92_*679+93dup	ENSP00000454782.1:n.*679+92_*679+93dup
ENST00000611625.4:c.2502+92_2502+93dup	ENSP00000481063.1:n.2502+92_2502+93dup
ENST00000612417.4:c.1853+3335_1853+3336dup	ENSP00000478360.1:n.1853+3335_1853+3336dup
ENST00000621016.4:c.1866-4314_1866-4313dup	ENSP00000480664.1:n.1866-4314_1866-4313dup
NM_004360.3:c.2439+92_2439+93dup , LRG_301t1:c.2439+92_2439+93dup	NP_004351.1:n.2439+92_2439+93dup
XM_011523488.1:c.1704+92_1704+93dup	XP_011521790.1:n.1704+92_1704+93dup
XM_011523489.1:c.1704+92_1704+93dup	XP_011521791.1:n.1704+92_1704+93dup
NM_001317184.1:c.2256+92_2256+93dup	NP_001304113.1:n.2256+92_2256+93dup
NM_001317185.1:c.891+92_891+93dup	NP_001304114.1:n.891+92_891+93dup
NM_001317186.1:c.474+92_474+93dup	NP_001304115.1:n.474+92_474+93dup
NM_004360.4:c.2439+92_2439+93dup	NP_004351.1:n.2439+92_2439+93dup
NM_004360.5:c.2439+92_2439+93dup MANE Select	NP_004351.1:n.2439+92_2439+93dup
NM_001317184.2:c.2256+92_2256+93dup	NP_001304113.1:n.2256+92_2256+93dup
NM_001317185.2:c.891+92_891+93dup	NP_001304114.1:n.891+92_891+93dup
NM_001317186.2:c.474+92_474+93dup	NP_001304115.1:n.474+92_474+93dup