Canonical Allele Identifier: CA2229914898
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737345C= , CM000678.2:g.68737345C= GRCh38
NC_000016.9:g.68771248C= , CM000678.1:g.68771248C= GRCh37
NC_000016.8:g.67328749C= NCBI36
NG_008021.1:g.5054C= , LRG_301:g.5054C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.-71C= MANE Select ENSP00000261769.4:n.-71C=
ENST00000261769.9:c.-71C= ENSP00000261769.4:n.-71C=
ENST00000566612.5:c.-71C= ENSP00000454782.1:n.-71C=
ENST00000611625.4:c.-71C= ENSP00000481063.1:n.-71C=
ENST00000612417.4:c.-71C= ENSP00000478360.1:n.-71C=
ENST00000621016.4:c.-71C= ENSP00000480664.1:n.-71C=
NM_004360.3:c.-71C= , LRG_301t1:c.-71C= NP_004351.1:n.-71C=
NM_001317184.1:c.-71C= NP_001304113.1:n.-71C=
NM_001317185.1:c.-1686C= NP_001304114.1:n.-1686C=
NM_001317186.1:c.-1890C= NP_001304115.1:n.-1890C=
NM_004360.4:c.-71C= NP_004351.1:n.-71C=
NM_004360.5:c.-71C= MANE Select NP_004351.1:n.-71C=
NM_001317184.2:c.-71C= NP_001304113.1:n.-71C=
NM_001317185.2:c.-1686C= NP_001304114.1:n.-1686C=
NM_001317186.2:c.-1890C= NP_001304115.1:n.-1890C=