Canonical Allele Identifier: CA2229914894
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737344T= , CM000678.2:g.68737344T= GRCh38
NC_000016.9:g.68771247T= , CM000678.1:g.68771247T= GRCh37
NC_000016.8:g.67328748T= NCBI36
NG_008021.1:g.5053T= , LRG_301:g.5053T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.-72T= MANE Select ENSP00000261769.4:n.-72T=
ENST00000261769.9:c.-72T= ENSP00000261769.4:n.-72T=
ENST00000566612.5:c.-72T= ENSP00000454782.1:n.-72T=
ENST00000611625.4:c.-72T= ENSP00000481063.1:n.-72T=
ENST00000612417.4:c.-72T= ENSP00000478360.1:n.-72T=
ENST00000621016.4:c.-72T= ENSP00000480664.1:n.-72T=
NM_004360.3:c.-72T= , LRG_301t1:c.-72T= NP_004351.1:n.-72T=
NM_001317184.1:c.-72T= NP_001304113.1:n.-72T=
NM_001317185.1:c.-1687T= NP_001304114.1:n.-1687T=
NM_001317186.1:c.-1891T= NP_001304115.1:n.-1891T=
NM_004360.4:c.-72T= NP_004351.1:n.-72T=
NM_004360.5:c.-72T= MANE Select NP_004351.1:n.-72T=
NM_001317184.2:c.-72T= NP_001304113.1:n.-72T=
NM_001317185.2:c.-1687T= NP_001304114.1:n.-1687T=
NM_001317186.2:c.-1891T= NP_001304115.1:n.-1891T=