Canonical Allele Identifier: CA2229965099
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68808535_68808536delinsGA , CM000678.2:g.68808535_68808536delinsGA GRCh38
NC_000016.9:g.68842438_68842439delinsGA , CM000678.1:g.68842438_68842439delinsGA GRCh37
NC_000016.8:g.67399939_67399940delinsGA NCBI36
NG_008021.1:g.76244_76245delinsGA , LRG_301:g.76244_76245delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.499_500delinsGA MANE Select ENSP00000261769.4:p.Glu167=
ENST00000261769.9:c.499_500delinsGA ENSP00000261769.4:p.Glu167=
ENST00000422392.6:c.499_500delinsGA ENSP00000414946.2:p.Glu167=
ENST00000561751.1:c.266_267delinsGA
ENST00000562836.5:n.570_571delinsGA
ENST00000564676.5:n.781_782delinsGA
ENST00000564745.1:n.494_495delinsGA
ENST00000566510.5:c.499_500delinsGA ENSP00000458139.1:p.Glu167=
ENST00000566612.5:c.499_500delinsGA ENSP00000454782.1:p.Glu167=
ENST00000567320.1:n.9_10delinsGA
ENST00000611625.4:c.499_500delinsGA ENSP00000481063.1:p.Glu167=
ENST00000612417.4:c.499_500delinsGA ENSP00000478360.1:p.Glu167=
ENST00000621016.4:c.499_500delinsGA ENSP00000480664.1:p.Glu167=
NM_004360.3:c.499_500delinsGA , LRG_301t1:c.499_500delinsGA NP_004351.1:p.Glu167=
XM_011523488.1:c.-237_-236delinsGA XP_011521790.1:n.-237_-236delinsGA
XM_011523489.1:c.-237_-236delinsGA XP_011521791.1:n.-237_-236delinsGA
NM_001317184.1:c.499_500delinsGA NP_001304113.1:p.Glu167=
NM_001317185.1:c.-1117_-1116delinsGA NP_001304114.1:n.-1117_-1116delinsGA
NM_001317186.1:c.-1321_-1320delinsGA NP_001304115.1:n.-1321_-1320delinsGA
NM_004360.4:c.499_500delinsGA NP_004351.1:p.Glu167=
NM_004360.5:c.499_500delinsGA MANE Select NP_004351.1:p.Glu167=
NM_001317184.2:c.499_500delinsGA NP_001304113.1:p.Glu167=
NM_001317185.2:c.-1117_-1116delinsGA NP_001304114.1:n.-1117_-1116delinsGA
NM_001317186.2:c.-1321_-1320delinsGA NP_001304115.1:n.-1321_-1320delinsGA