Canonical Allele Identifier: CA2633933528

Gene: CDH1

Linked Data

• gnomAD v4: 16-68834675-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68834677del , CM000678.2:g.68834677del	GRCh38
NC_000016.9:g.68868580del , CM000678.1:g.68868580del	GRCh37
NC_000016.8:g.67426081del	NCBI36
NG_008021.1:g.102386del , LRG_301:g.102386del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.*1178del MANE Select	ENSP00000261769.4:n.*1178del
ENST00000261769.9:c.*1178del	ENSP00000261769.4:n.*1178del
ENST00000566612.5:c.*2067del	ENSP00000454782.1:n.*2067del
ENST00000611625.4:c.*1178del	ENSP00000481063.1:n.*1178del
ENST00000621016.4:c.*396del	ENSP00000480664.1:n.*396del
NM_004360.3:c.*1178del , LRG_301t1:c.*1178del	NP_004351.1:n.*1178del
XM_011523488.1:c.*1178del	XP_011521790.1:n.*1178del
XM_011523489.1:c.*1178del	XP_011521791.1:n.*1178del
NM_001317184.1:c.*1178del	NP_001304113.1:n.*1178del
NM_001317185.1:c.*1178del	NP_001304114.1:n.*1178del
NM_001317186.1:c.*1178del	NP_001304115.1:n.*1178del
NM_004360.4:c.*1178del	NP_004351.1:n.*1178del
NM_004360.5:c.*1178del MANE Select	NP_004351.1:n.*1178del
NM_001317184.2:c.*1178del	NP_001304113.1:n.*1178del
NM_001317185.2:c.*1178del	NP_001304114.1:n.*1178del
NM_001317186.2:c.*1178del	NP_001304115.1:n.*1178del