Canonical Allele Identifier: CA2229915008
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737381C= , CM000678.2:g.68737381C= GRCh38
NC_000016.9:g.68771284C= , CM000678.1:g.68771284C= GRCh37
NC_000016.8:g.67328785C= NCBI36
NG_008021.1:g.5090C= , LRG_301:g.5090C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.-35C= MANE Select ENSP00000261769.4:n.-35C=
ENST00000261769.9:c.-35C= ENSP00000261769.4:n.-35C=
ENST00000422392.6:c.-35C= ENSP00000414946.2:n.-35C=
ENST00000566510.5:c.-35C= ENSP00000458139.1:n.-35C=
ENST00000566612.5:c.-35C= ENSP00000454782.1:n.-35C=
ENST00000611625.4:c.-35C= ENSP00000481063.1:n.-35C=
ENST00000612417.4:c.-35C= ENSP00000478360.1:n.-35C=
ENST00000621016.4:c.-35C= ENSP00000480664.1:n.-35C=
NM_004360.3:c.-35C= , LRG_301t1:c.-35C= NP_004351.1:n.-35C=
NM_001317184.1:c.-35C= NP_001304113.1:n.-35C=
NM_001317185.1:c.-1650C= NP_001304114.1:n.-1650C=
NM_001317186.1:c.-1854C= NP_001304115.1:n.-1854C=
NM_004360.4:c.-35C= NP_004351.1:n.-35C=
NM_004360.5:c.-35C= MANE Select NP_004351.1:n.-35C=
NM_001317184.2:c.-35C= NP_001304113.1:n.-35C=
NM_001317185.2:c.-1650C= NP_001304114.1:n.-1650C=
NM_001317186.2:c.-1854C= NP_001304115.1:n.-1854C=