Canonical Allele Identifier: CA645596585

Gene: CDH1

Linked Data

• COSMIC: COSM4777510

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68801697_68801698insCT , CM000678.2:g.68801697_68801698insCT	GRCh38
NC_000016.9:g.68835600_68835601insCT , CM000678.1:g.68835600_68835601insCT	GRCh37
NC_000016.8:g.67393101_67393102insCT	NCBI36
NG_008021.1:g.69406_69407insCT , LRG_301:g.69406_69407insCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.191_192insCT MANE Select	ENSP00000261769.4:p.Gln64HisfsTer2
ENST00000261769.9:c.191_192insCT	ENSP00000261769.4:p.Gln64HisfsTer2
ENST00000422392.6:c.191_192insCT	ENSP00000414946.2:p.Gln64HisfsTer2
ENST00000562836.5:n.262_263insCT
ENST00000564676.5:n.473_474insCT
ENST00000564745.1:n.186_187insCT
ENST00000566510.5:c.191_192insCT	ENSP00000458139.1:p.Gln64HisfsTer2
ENST00000566612.5:c.191_192insCT	ENSP00000454782.1:p.Gln64HisfsTer2
ENST00000611625.4:c.191_192insCT	ENSP00000481063.1:p.Gln64HisfsTer2
ENST00000612417.4:c.191_192insCT	ENSP00000478360.1:p.Gln64HisfsTer2
ENST00000621016.4:c.191_192insCT	ENSP00000480664.1:p.Gln64HisfsTer2
NM_004360.3:c.191_192insCT , LRG_301t1:c.191_192insCT	NP_004351.1:p.Gln64HisfsTer2
XM_011523488.1:c.-545_-544insCT	XP_011521790.1:n.-545_-544insCT
XM_011523489.1:c.-545_-544insCT	XP_011521791.1:n.-545_-544insCT
NM_001317184.1:c.191_192insCT	NP_001304113.1:p.Gln64HisfsTer2
NM_001317185.1:c.-1425_-1424insCT	NP_001304114.1:n.-1425_-1424insCT
NM_001317186.1:c.-1629_-1628insCT	NP_001304115.1:n.-1629_-1628insCT
NM_004360.4:c.191_192insCT	NP_004351.1:p.Gln64HisfsTer2
NM_004360.5:c.191_192insCT MANE Select	NP_004351.1:p.Gln64HisfsTer2
NM_001317184.2:c.191_192insCT	NP_001304113.1:p.Gln64HisfsTer2
NM_001317185.2:c.-1425_-1424insCT	NP_001304114.1:n.-1425_-1424insCT
NM_001317186.2:c.-1629_-1628insCT	NP_001304115.1:n.-1629_-1628insCT