Canonical Allele Identifier: CA645569996

Gene: CDH1

Linked Data

• COSMIC: COSM219704

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68738334_68738337delinsGTG , CM000678.2:g.68738334_68738337delinsGTG	GRCh38
NC_000016.9:g.68772237_68772240delinsGTG , CM000678.1:g.68772237_68772240delinsGTG	GRCh37
NC_000016.8:g.67329738_67329741delinsGTG	NCBI36
NG_008021.1:g.6043_6046delinsGTG , LRG_301:g.6043_6046delinsGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.86_89delinsGTG MANE Select	ENSP00000261769.4:p.His29ArgfsTer27
ENST00000261769.9:c.86_89delinsGTG	ENSP00000261769.4:p.His29ArgfsTer27
ENST00000422392.6:c.86_89delinsGTG	ENSP00000414946.2:p.His29ArgfsTer27
ENST00000566510.5:c.86_89delinsGTG	ENSP00000458139.1:p.His29ArgfsTer27
ENST00000566612.5:c.86_89delinsGTG	ENSP00000454782.1:p.His29ArgfsTer27
ENST00000611625.4:c.86_89delinsGTG	ENSP00000481063.1:p.His29ArgfsTer27
ENST00000612417.4:c.86_89delinsGTG	ENSP00000478360.1:p.His29ArgfsTer27
ENST00000621016.4:c.86_89delinsGTG	ENSP00000480664.1:p.His29ArgfsTer27
NM_004360.3:c.86_89delinsGTG , LRG_301t1:c.86_89delinsGTG	NP_004351.1:p.His29ArgfsTer27
NM_001317184.1:c.86_89delinsGTG	NP_001304113.1:p.His29ArgfsTer27
NM_001317185.1:c.-1530_-1527delinsGTG	NP_001304114.1:n.-1530_-1527delinsGTG
NM_001317186.1:c.-1734_-1731delinsGTG	NP_001304115.1:n.-1734_-1731delinsGTG
NM_004360.4:c.86_89delinsGTG	NP_004351.1:p.His29ArgfsTer27
NM_004360.5:c.86_89delinsGTG MANE Select	NP_004351.1:p.His29ArgfsTer27
NM_001317184.2:c.86_89delinsGTG	NP_001304113.1:p.His29ArgfsTer27
NM_001317185.2:c.-1530_-1527delinsGTG	NP_001304114.1:n.-1530_-1527delinsGTG
NM_001317186.2:c.-1734_-1731delinsGTG	NP_001304115.1:n.-1734_-1731delinsGTG