Canonical Allele Identifier: CA2229975170
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829771_68829772delinsGA , CM000678.2:g.68829771_68829772delinsGA GRCh38
NC_000016.9:g.68863674_68863675delinsGA , CM000678.1:g.68863674_68863675delinsGA GRCh37
NC_000016.8:g.67421175_67421176delinsGA NCBI36
NG_008021.1:g.97480_97481delinsGA , LRG_301:g.97480_97481delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2413_2414delinsGA MANE Select ENSP00000261769.4:p.Asp805=
ENST00000261769.9:c.2413_2414delinsGA ENSP00000261769.4:p.Asp805=
ENST00000422392.6:c.2230_2231delinsGA ENSP00000414946.2:p.Asp744=
ENST00000562118.1:n.631_632delinsGA
ENST00000562836.5:n.2484_2485delinsGA
ENST00000566510.5:c.*1079_*1080delinsGA ENSP00000458139.1:n.*1079_*1080delinsGA
ENST00000566612.5:c.*653_*654delinsGA ENSP00000454782.1:n.*653_*654delinsGA
ENST00000611625.4:c.2476_2477delinsGA ENSP00000481063.1:p.Asp826=
ENST00000612417.4:c.1853+3217_1853+3218delinsGA ENSP00000478360.1:n.1853+3217_1853+3218delinsGA
ENST00000621016.4:c.1866-4432_1866-4431delinsGA ENSP00000480664.1:n.1866-4432_1866-4431delinsGA
NM_004360.3:c.2413_2414delinsGA , LRG_301t1:c.2413_2414delinsGA NP_004351.1:p.Asp805=
XM_011523488.1:c.1678_1679delinsGA XP_011521790.1:p.Asp560=
XM_011523489.1:c.1678_1679delinsGA XP_011521791.1:p.Asp560=
NM_001317184.1:c.2230_2231delinsGA NP_001304113.1:p.Asp744=
NM_001317185.1:c.865_866delinsGA NP_001304114.1:p.Asp289=
NM_001317186.1:c.448_449delinsGA NP_001304115.1:p.Asp150=
NM_004360.4:c.2413_2414delinsGA NP_004351.1:p.Asp805=
NM_004360.5:c.2413_2414delinsGA MANE Select NP_004351.1:p.Asp805=
NM_001317184.2:c.2230_2231delinsGA NP_001304113.1:p.Asp744=
NM_001317185.2:c.865_866delinsGA NP_001304114.1:p.Asp289=
NM_001317186.2:c.448_449delinsGA NP_001304115.1:p.Asp150=