Canonical Allele Identifier: CA2633931678

Gene: CDH1

Linked Data

• gnomAD v4: 16-68819129-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68819130dup , CM000678.2:g.68819130dup	GRCh38
NC_000016.9:g.68853033dup , CM000678.1:g.68853033dup	GRCh37
NC_000016.8:g.67410534dup	NCBI36
NG_008021.1:g.86839dup , LRG_301:g.86839dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1566-150dup MANE Select	ENSP00000261769.4:n.1566-150dup
ENST00000261769.9:c.1566-150dup	ENSP00000261769.4:n.1566-150dup
ENST00000422392.6:c.1383-150dup	ENSP00000414946.2:n.1383-150dup
ENST00000562836.5:n.1637-150dup
ENST00000566510.5:c.*232-150dup	ENSP00000458139.1:n.*232-150dup
ENST00000566612.5:c.1566-2871dup	ENSP00000454782.1:n.1566-2871dup
ENST00000611625.4:c.1629-150dup	ENSP00000481063.1:n.1629-150dup
ENST00000612417.4:c.1566-150dup	ENSP00000478360.1:n.1566-150dup
ENST00000621016.4:c.1566-150dup	ENSP00000480664.1:n.1566-150dup
NM_004360.3:c.1566-150dup , LRG_301t1:c.1566-150dup	NP_004351.1:n.1566-150dup
XM_011523488.1:c.831-150dup	XP_011521790.1:n.831-150dup
XM_011523489.1:c.831-150dup	XP_011521791.1:n.831-150dup
NM_001317184.1:c.1383-150dup	NP_001304113.1:n.1383-150dup
NM_001317185.1:c.18-150dup	NP_001304114.1:n.18-150dup
NM_001317186.1:c.-254-2871dup	NP_001304115.1:n.-254-2871dup
NM_004360.4:c.1566-150dup	NP_004351.1:n.1566-150dup
NM_004360.5:c.1566-150dup MANE Select	NP_004351.1:n.1566-150dup
NM_001317184.2:c.1383-150dup	NP_001304113.1:n.1383-150dup
NM_001317185.2:c.18-150dup	NP_001304114.1:n.18-150dup
NM_001317186.2:c.-254-2871dup	NP_001304115.1:n.-254-2871dup