Canonical Allele Identifier: CA2633898094

Gene: CDH1

Linked Data

• gnomAD v4: 16-68737393-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737394del , CM000678.2:g.68737394del	GRCh38
NC_000016.9:g.68771297del , CM000678.1:g.68771297del	GRCh37
NC_000016.8:g.67328798del	NCBI36
NG_008021.1:g.5103del , LRG_301:g.5103del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.-22del MANE Select	ENSP00000261769.4:n.-22del
ENST00000261769.9:c.-22del	ENSP00000261769.4:n.-22del
ENST00000422392.6:c.-22del	ENSP00000414946.2:n.-22del
ENST00000566510.5:c.-22del	ENSP00000458139.1:n.-22del
ENST00000566612.5:c.-22del	ENSP00000454782.1:n.-22del
ENST00000611625.4:c.-22del	ENSP00000481063.1:n.-22del
ENST00000612417.4:c.-22del	ENSP00000478360.1:n.-22del
ENST00000621016.4:c.-22del	ENSP00000480664.1:n.-22del
NM_004360.3:c.-22del , LRG_301t1:c.-22del	NP_004351.1:n.-22del
NM_001317184.1:c.-22del	NP_001304113.1:n.-22del
NM_001317185.1:c.-1637del	NP_001304114.1:n.-1637del
NM_001317186.1:c.-1841del	NP_001304115.1:n.-1841del
NM_004360.4:c.-22del	NP_004351.1:n.-22del
NM_004360.5:c.-22del MANE Select	NP_004351.1:n.-22del
NM_001317184.2:c.-22del	NP_001304113.1:n.-22del
NM_001317185.2:c.-1637del	NP_001304114.1:n.-1637del
NM_001317186.2:c.-1841del	NP_001304115.1:n.-1841del