Canonical Allele Identifier: CA2229978129
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833318C= , CM000678.2:g.68833318C= GRCh38
NC_000016.9:g.68867221C= , CM000678.1:g.68867221C= GRCh37
NC_000016.8:g.67424722C= NCBI36
NG_008021.1:g.101027C= , LRG_301:g.101027C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2468C= MANE Select ENSP00000261769.4:p.Thr823=
ENST00000261769.9:c.2468C= ENSP00000261769.4:p.Thr823=
ENST00000422392.6:c.2285C= ENSP00000414946.2:p.Thr762=
ENST00000562118.1:n.686C=
ENST00000562836.5:n.2539C=
ENST00000566510.5:c.*1134C= ENSP00000458139.1:n.*1134C=
ENST00000566612.5:c.*708C= ENSP00000454782.1:n.*708C=
ENST00000611625.4:c.2531C= ENSP00000481063.1:p.Thr844=
ENST00000612417.4:c.1854-873C= ENSP00000478360.1:n.1854-873C=
ENST00000621016.4:c.1866-885C= ENSP00000480664.1:n.1866-885C=
NM_004360.3:c.2468C= , LRG_301t1:c.2468C= NP_004351.1:p.Thr823=
XM_011523488.1:c.1733C= XP_011521790.1:p.Thr578=
XM_011523489.1:c.1733C= XP_011521791.1:p.Thr578=
NM_001317184.1:c.2285C= NP_001304113.1:p.Thr762=
NM_001317185.1:c.920C= NP_001304114.1:p.Thr307=
NM_001317186.1:c.503C= NP_001304115.1:p.Thr168=
NM_004360.4:c.2468C= NP_004351.1:p.Thr823=
NM_004360.5:c.2468C= MANE Select NP_004351.1:p.Thr823=
NM_001317184.2:c.2285C= NP_001304113.1:p.Thr762=
NM_001317185.2:c.920C= NP_001304114.1:p.Thr307=
NM_001317186.2:c.503C= NP_001304115.1:p.Thr168=