Canonical Allele Identifier: CA2229975345
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829842C= , CM000678.2:g.68829842C= GRCh38
NC_000016.9:g.68863745C= , CM000678.1:g.68863745C= GRCh37
NC_000016.8:g.67421246C= NCBI36
NG_008021.1:g.97551C= , LRG_301:g.97551C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+45C= MANE Select ENSP00000261769.4:n.2439+45C=
ENST00000261769.9:c.2439+45C= ENSP00000261769.4:n.2439+45C=
ENST00000422392.6:c.2256+45C= ENSP00000414946.2:n.2256+45C=
ENST00000562118.1:n.657+45C=
ENST00000562836.5:n.2510+45C=
ENST00000566510.5:c.*1105+45C= ENSP00000458139.1:n.*1105+45C=
ENST00000566612.5:c.*679+45C= ENSP00000454782.1:n.*679+45C=
ENST00000611625.4:c.2502+45C= ENSP00000481063.1:n.2502+45C=
ENST00000612417.4:c.1853+3288C= ENSP00000478360.1:n.1853+3288C=
ENST00000621016.4:c.1866-4361C= ENSP00000480664.1:n.1866-4361C=
NM_004360.3:c.2439+45C= , LRG_301t1:c.2439+45C= NP_004351.1:n.2439+45C=
XM_011523488.1:c.1704+45C= XP_011521790.1:n.1704+45C=
XM_011523489.1:c.1704+45C= XP_011521791.1:n.1704+45C=
NM_001317184.1:c.2256+45C= NP_001304113.1:n.2256+45C=
NM_001317185.1:c.891+45C= NP_001304114.1:n.891+45C=
NM_001317186.1:c.474+45C= NP_001304115.1:n.474+45C=
NM_004360.4:c.2439+45C= NP_004351.1:n.2439+45C=
NM_004360.5:c.2439+45C= MANE Select NP_004351.1:n.2439+45C=
NM_001317184.2:c.2256+45C= NP_001304113.1:n.2256+45C=
NM_001317185.2:c.891+45C= NP_001304114.1:n.891+45C=
NM_001317186.2:c.474+45C= NP_001304115.1:n.474+45C=