Canonical Allele Identifier: CA2229975155
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829769C= , CM000678.2:g.68829769C= GRCh38
NC_000016.9:g.68863672C= , CM000678.1:g.68863672C= GRCh37
NC_000016.8:g.67421173C= NCBI36
NG_008021.1:g.97478C= , LRG_301:g.97478C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2411C= MANE Select ENSP00000261769.4:p.Pro804=
ENST00000261769.9:c.2411C= ENSP00000261769.4:p.Pro804=
ENST00000422392.6:c.2228C= ENSP00000414946.2:p.Pro743=
ENST00000562118.1:n.629C=
ENST00000562836.5:n.2482C=
ENST00000566510.5:c.*1077C= ENSP00000458139.1:n.*1077C=
ENST00000566612.5:c.*651C= ENSP00000454782.1:n.*651C=
ENST00000611625.4:c.2474C= ENSP00000481063.1:p.Pro825=
ENST00000612417.4:c.1853+3215C= ENSP00000478360.1:n.1853+3215C=
ENST00000621016.4:c.1866-4434C= ENSP00000480664.1:n.1866-4434C=
NM_004360.3:c.2411C= , LRG_301t1:c.2411C= NP_004351.1:p.Pro804=
XM_011523488.1:c.1676C= XP_011521790.1:p.Pro559=
XM_011523489.1:c.1676C= XP_011521791.1:p.Pro559=
NM_001317184.1:c.2228C= NP_001304113.1:p.Pro743=
NM_001317185.1:c.863C= NP_001304114.1:p.Pro288=
NM_001317186.1:c.446C= NP_001304115.1:p.Pro149=
NM_004360.4:c.2411C= NP_004351.1:p.Pro804=
NM_004360.5:c.2411C= MANE Select NP_004351.1:p.Pro804=
NM_001317184.2:c.2228C= NP_001304113.1:p.Pro743=
NM_001317185.2:c.863C= NP_001304114.1:p.Pro288=
NM_001317186.2:c.446C= NP_001304115.1:p.Pro149=