Canonical Allele Identifier: CA2229958267

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68801919_68801935delinsTCGCTGTTGTTTTAGTG , CM000678.2:g.68801919_68801935delinsTCGCTGTTGTTTTAGTG	GRCh38
NC_000016.9:g.68835822_68835838delinsTCGCTGTTGTTTTAGTG , CM000678.1:g.68835822_68835838delinsTCGCTGTTGTTTTAGTG	GRCh37
NC_000016.8:g.67393323_67393339delinsTCGCTGTTGTTTTAGTG	NCBI36
NG_008021.1:g.69628_69644delinsTCGCTGTTGTTTTAGTG , LRG_301:g.69628_69644delinsTCGCTGTTGTTTTAGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.387+26_387+42delinsTCGCTGTTGTTTTAGTG MANE Select	ENSP00000261769.4:n.387+26_387+42delinsTC...
ENST00000261769.9:c.387+26_387+42delinsTCGCTGTTGTTTTAGTG	ENSP00000261769.4:n.387+26_387+42delinsTC...
ENST00000422392.6:c.387+26_387+42delinsTCGCTGTTGTTTTAGTG	ENSP00000414946.2:n.387+26_387+42delinsTC...
ENST00000561751.1:c.154+26_154+42delinsTCGCTGTTGTTTTAGTG
ENST00000562836.5:n.458+26_458+42delinsTCGCTGTTGTTTTAGTG
ENST00000564676.5:n.669+26_669+42delinsTCGCTGTTGTTTTAGTG
ENST00000564745.1:n.382+26_382+42delinsTCGCTGTTGTTTTAGTG
ENST00000566510.5:c.387+26_387+42delinsTCGCTGTTGTTTTAGTG	ENSP00000458139.1:n.387+26_387+42delinsTC...
ENST00000566612.5:c.387+26_387+42delinsTCGCTGTTGTTTTAGTG	ENSP00000454782.1:n.387+26_387+42delinsTC...
ENST00000611625.4:c.387+26_387+42delinsTCGCTGTTGTTTTAGTG	ENSP00000481063.1:n.387+26_387+42delinsTC...
ENST00000612417.4:c.387+26_387+42delinsTCGCTGTTGTTTTAGTG	ENSP00000478360.1:n.387+26_387+42delinsTC...
ENST00000621016.4:c.387+26_387+42delinsTCGCTGTTGTTTTAGTG	ENSP00000480664.1:n.387+26_387+42delinsTC...
NM_004360.3:c.387+26_387+42delinsTCGCTGTTGTTTTAGTG , LRG_301t1:c.387+26_387+42delinsTCGCTGTTGTTTTAGTG	NP_004351.1:n.387+26_387+42delinsTCGCTGTT...
XM_011523488.1:c.-349+26_-349+42delinsTCGCTGTTGTTTTAGTG	XP_011521790.1:n.-349+26_-349+42delinsTCG...
XM_011523489.1:c.-349+26_-349+42delinsTCGCTGTTGTTTTAGTG	XP_011521791.1:n.-349+26_-349+42delinsTCG...
NM_001317184.1:c.387+26_387+42delinsTCGCTGTTGTTTTAGTG	NP_001304113.1:n.387+26_387+42delinsTCGCT...
NM_001317185.1:c.-1229+26_-1229+42delinsTCGCTGTTGTTTTAGTG	NP_001304114.1:n.-1229+26_-1229+42delinsT...
NM_001317186.1:c.-1433+26_-1433+42delinsTCGCTGTTGTTTTAGTG	NP_001304115.1:n.-1433+26_-1433+42delinsT...
NM_004360.4:c.387+26_387+42delinsTCGCTGTTGTTTTAGTG	NP_004351.1:n.387+26_387+42delinsTCGCTGTT...
NM_004360.5:c.387+26_387+42delinsTCGCTGTTGTTTTAGTG MANE Select	NP_004351.1:n.387+26_387+42delinsTCGCTGTT...
NM_001317184.2:c.387+26_387+42delinsTCGCTGTTGTTTTAGTG	NP_001304113.1:n.387+26_387+42delinsTCGCT...
NM_001317185.2:c.-1229+26_-1229+42delinsTCGCTGTTGTTTTAGTG	NP_001304114.1:n.-1229+26_-1229+42delinsT...
NM_001317186.2:c.-1433+26_-1433+42delinsTCGCTGTTGTTTTAGTG	NP_001304115.1:n.-1433+26_-1433+42delinsT...