Canonical Allele Identifier: CA2229975201
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829783_68829785delinsAAT , CM000678.2:g.68829783_68829785delinsAAT GRCh38
NC_000016.9:g.68863686_68863688delinsAAT , CM000678.1:g.68863686_68863688delinsAAT GRCh37
NC_000016.8:g.67421187_67421189delinsAAT NCBI36
NG_008021.1:g.97492_97494delinsAAT , LRG_301:g.97492_97494delinsAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2425_2427delinsAAT MANE Select ENSP00000261769.4:p.Asn809=
ENST00000261769.9:c.2425_2427delinsAAT ENSP00000261769.4:p.Asn809=
ENST00000422392.6:c.2242_2244delinsAAT ENSP00000414946.2:p.Asn748=
ENST00000562118.1:n.643_645delinsAAT
ENST00000562836.5:n.2496_2498delinsAAT
ENST00000566510.5:c.*1091_*1093delinsAAT ENSP00000458139.1:n.*1091_*1093delinsAAT
ENST00000566612.5:c.*665_*667delinsAAT ENSP00000454782.1:n.*665_*667delinsAAT
ENST00000611625.4:c.2488_2490delinsAAT ENSP00000481063.1:p.Asn830=
ENST00000612417.4:c.1853+3229_1853+3231delinsAAT ENSP00000478360.1:n.1853+3229_1853+3231delinsAAT
ENST00000621016.4:c.1866-4420_1866-4418delinsAAT ENSP00000480664.1:n.1866-4420_1866-4418delinsAAT
NM_004360.3:c.2425_2427delinsAAT , LRG_301t1:c.2425_2427delinsAAT NP_004351.1:p.Asn809=
XM_011523488.1:c.1690_1692delinsAAT XP_011521790.1:p.Asn564=
XM_011523489.1:c.1690_1692delinsAAT XP_011521791.1:p.Asn564=
NM_001317184.1:c.2242_2244delinsAAT NP_001304113.1:p.Asn748=
NM_001317185.1:c.877_879delinsAAT NP_001304114.1:p.Asn293=
NM_001317186.1:c.460_462delinsAAT NP_001304115.1:p.Asn154=
NM_004360.4:c.2425_2427delinsAAT NP_004351.1:p.Asn809=
NM_004360.5:c.2425_2427delinsAAT MANE Select NP_004351.1:p.Asn809=
NM_001317184.2:c.2242_2244delinsAAT NP_001304113.1:p.Asn748=
NM_001317185.2:c.877_879delinsAAT NP_001304114.1:p.Asn293=
NM_001317186.2:c.460_462delinsAAT NP_001304115.1:p.Asn154=