Canonical Allele Identifier: CA919732079

Gene: CDH1

Linked Data

• dbSNP Id: rs1567512205

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822049_68822051del , CM000678.2:g.68822049_68822051del	GRCh38
NC_000016.9:g.68855952_68855954del , CM000678.1:g.68855952_68855954del	GRCh37
NC_000016.8:g.67413453_67413455del	NCBI36
NG_008021.1:g.89758_89760del , LRG_301:g.89758_89760del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1760_1762del MANE Select	ENSP00000261769.4:p.Asp587del
ENST00000261769.9:c.1760_1762del	ENSP00000261769.4:p.Asp587del
ENST00000422392.6:c.1577_1579del	ENSP00000414946.2:p.Asp526del
ENST00000562836.5:n.1831_1833del
ENST00000566510.5:c.*426_*428del	ENSP00000458139.1:n.*426_*428del
ENST00000566612.5:c.1614_*2del	ENSP00000454782.1:n.[c.1614_*2del;Ter538CysextTer3]
ENST00000611625.4:c.1823_1825del	ENSP00000481063.1:p.Asp608del
ENST00000612417.4:c.1760_1762del	ENSP00000478360.1:p.Asp587del
ENST00000621016.4:c.1760_1762del	ENSP00000480664.1:p.Asp587del
NM_004360.3:c.1760_1762del , LRG_301t1:c.1760_1762del	NP_004351.1:p.Asp587del
XM_011523488.1:c.1025_1027del	XP_011521790.1:p.Asp342del
XM_011523489.1:c.1025_1027del	XP_011521791.1:p.Asp342del
NM_001317184.1:c.1577_1579del	NP_001304113.1:p.Asp526del
NM_001317185.1:c.212_214del	NP_001304114.1:p.Asp71del
NM_001317186.1:c.-206_-204del	NP_001304115.1:n.-206_-204del
NM_004360.4:c.1760_1762del	NP_004351.1:p.Asp587del
NM_004360.5:c.1760_1762del MANE Select	NP_004351.1:p.Asp587del
NM_001317184.2:c.1577_1579del	NP_001304113.1:p.Asp526del
NM_001317185.2:c.212_214del	NP_001304114.1:p.Asp71del
NM_001317186.2:c.-206_-204del	NP_001304115.1:n.-206_-204del