Canonical Allele Identifier: CA2633899717

Gene: CDH1

Linked Data

• gnomAD v4: 16-68738281-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68738284del , CM000678.2:g.68738284del	GRCh38
NC_000016.9:g.68772187del , CM000678.1:g.68772187del	GRCh37
NC_000016.8:g.67329688del	NCBI36
NG_008021.1:g.5993del , LRG_301:g.5993del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.49-13del MANE Select	ENSP00000261769.4:n.49-13del
ENST00000261769.9:c.49-13del	ENSP00000261769.4:n.49-13del
ENST00000422392.6:c.49-13del	ENSP00000414946.2:n.49-13del
ENST00000566510.5:c.49-13del	ENSP00000458139.1:n.49-13del
ENST00000566612.5:c.49-13del	ENSP00000454782.1:n.49-13del
ENST00000611625.4:c.49-13del	ENSP00000481063.1:n.49-13del
ENST00000612417.4:c.49-13del	ENSP00000478360.1:n.49-13del
ENST00000621016.4:c.49-13del	ENSP00000480664.1:n.49-13del
NM_004360.3:c.49-13del , LRG_301t1:c.49-13del	NP_004351.1:n.49-13del
NM_001317184.1:c.49-13del	NP_001304113.1:n.49-13del
NM_001317185.1:c.-1567-13del	NP_001304114.1:n.-1567-13del
NM_001317186.1:c.-1771-13del	NP_001304115.1:n.-1771-13del
NM_004360.4:c.49-13del	NP_004351.1:n.49-13del
NM_004360.5:c.49-13del MANE Select	NP_004351.1:n.49-13del
NM_001317184.2:c.49-13del	NP_001304113.1:n.49-13del
NM_001317185.2:c.-1567-13del	NP_001304114.1:n.-1567-13del
NM_001317186.2:c.-1771-13del	NP_001304115.1:n.-1771-13del