Canonical Allele Identifier: CA2229967035
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810267C= , CM000678.2:g.68810267C= GRCh38
NC_000016.9:g.68844170C= , CM000678.1:g.68844170C= GRCh37
NC_000016.8:g.67401671C= NCBI36
NG_008021.1:g.77976C= , LRG_301:g.77976C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.758C= MANE Select ENSP00000261769.4:p.Thr253=
ENST00000261769.9:c.758C= ENSP00000261769.4:p.Thr253=
ENST00000422392.6:c.758C= ENSP00000414946.2:p.Thr253=
ENST00000561751.1:c.455-1417C=
ENST00000562836.5:n.829C=
ENST00000566510.5:c.602C= ENSP00000458139.1:p.Thr201=
ENST00000566612.5:c.758C= ENSP00000454782.1:p.Thr253=
ENST00000611625.4:c.758C= ENSP00000481063.1:p.Thr253=
ENST00000612417.4:c.758C= ENSP00000478360.1:p.Thr253=
ENST00000621016.4:c.758C= ENSP00000480664.1:p.Thr253=
NM_004360.3:c.758C= , LRG_301t1:c.758C= NP_004351.1:p.Thr253=
XM_011523488.1:c.23C= XP_011521790.1:p.Thr8=
XM_011523489.1:c.23C= XP_011521791.1:p.Thr8=
NM_001317184.1:c.758C= NP_001304113.1:p.Thr253=
NM_001317185.1:c.-858C= NP_001304114.1:n.-858C=
NM_001317186.1:c.-1062C= NP_001304115.1:n.-1062C=
NM_004360.4:c.758C= NP_004351.1:p.Thr253=
NM_004360.5:c.758C= MANE Select NP_004351.1:p.Thr253=
NM_001317184.2:c.758C= NP_001304113.1:p.Thr253=
NM_001317185.2:c.-858C= NP_001304114.1:n.-858C=
NM_001317186.2:c.-1062C= NP_001304115.1:n.-1062C=