Canonical Allele Identifier: CA2229978175
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819421C= , CM000678.2:g.68819421C= GRCh38
NC_000016.9:g.68853324C= , CM000678.1:g.68853324C= GRCh37
NC_000016.8:g.67410825C= NCBI36
NG_008021.1:g.87130C= , LRG_301:g.87130C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1707C= MANE Select ENSP00000261769.4:p.Asp569=
ENST00000261769.9:c.1707C= ENSP00000261769.4:p.Asp569=
ENST00000422392.6:c.1524C= ENSP00000414946.2:p.Asp508=
ENST00000562836.5:n.1778C=
ENST00000566510.5:c.*373C= ENSP00000458139.1:n.*373C=
ENST00000566612.5:c.1566-2580C= ENSP00000454782.1:n.1566-2580C=
ENST00000611625.4:c.1770C= ENSP00000481063.1:p.Asp590=
ENST00000612417.4:c.1707C= ENSP00000478360.1:p.Asp569=
ENST00000621016.4:c.1707C= ENSP00000480664.1:p.Asp569=
NM_004360.3:c.1707C= , LRG_301t1:c.1707C= NP_004351.1:p.Asp569=
XM_011523488.1:c.972C= XP_011521790.1:p.Asp324=
XM_011523489.1:c.972C= XP_011521791.1:p.Asp324=
NM_001317184.1:c.1524C= NP_001304113.1:p.Asp508=
NM_001317185.1:c.159C= NP_001304114.1:p.Asp53=
NM_001317186.1:c.-254-2580C= NP_001304115.1:n.-254-2580C=
NM_004360.4:c.1707C= NP_004351.1:p.Asp569=
NM_004360.5:c.1707C= MANE Select NP_004351.1:p.Asp569=
NM_001317184.2:c.1524C= NP_001304113.1:p.Asp508=
NM_001317185.2:c.159C= NP_001304114.1:p.Asp53=
NM_001317186.2:c.-254-2580C= NP_001304115.1:n.-254-2580C=