Canonical Allele Identifier: CA2633899918

Gene: CDH1

Linked Data

• gnomAD v4: 16-68738331-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68738333del , CM000678.2:g.68738333del	GRCh38
NC_000016.9:g.68772236del , CM000678.1:g.68772236del	GRCh37
NC_000016.8:g.67329737del	NCBI36
NG_008021.1:g.6042del , LRG_301:g.6042del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.85del MANE Select	ENSP00000261769.4:p.His29ThrfsTer27
ENST00000261769.9:c.85del	ENSP00000261769.4:p.His29ThrfsTer27
ENST00000422392.6:c.85del	ENSP00000414946.2:p.His29ThrfsTer27
ENST00000566510.5:c.85del	ENSP00000458139.1:p.His29ThrfsTer27
ENST00000566612.5:c.85del	ENSP00000454782.1:p.His29ThrfsTer27
ENST00000611625.4:c.85del	ENSP00000481063.1:p.His29ThrfsTer27
ENST00000612417.4:c.85del	ENSP00000478360.1:p.His29ThrfsTer27
ENST00000621016.4:c.85del	ENSP00000480664.1:p.His29ThrfsTer27
NM_004360.3:c.85del , LRG_301t1:c.85del	NP_004351.1:p.His29ThrfsTer27
NM_001317184.1:c.85del	NP_001304113.1:p.His29ThrfsTer27
NM_001317185.1:c.-1531del	NP_001304114.1:n.-1531del
NM_001317186.1:c.-1735del	NP_001304115.1:n.-1735del
NM_004360.4:c.85del	NP_004351.1:p.His29ThrfsTer27
NM_004360.5:c.85del MANE Select	NP_004351.1:p.His29ThrfsTer27
NM_001317184.2:c.85del	NP_001304113.1:p.His29ThrfsTer27
NM_001317185.2:c.-1531del	NP_001304114.1:n.-1531del
NM_001317186.2:c.-1735del	NP_001304115.1:n.-1735del