Canonical Allele Identifier: CA2229991969
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829651A= , CM000678.2:g.68829651A= GRCh38
NC_000016.9:g.68863554A= , CM000678.1:g.68863554A= GRCh37
NC_000016.8:g.67421055A= NCBI36
NG_008021.1:g.97360A= , LRG_301:g.97360A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2296-3A= MANE Select ENSP00000261769.4:n.2296-3A=
ENST00000261769.9:c.2296-3A= ENSP00000261769.4:n.2296-3A=
ENST00000422392.6:c.2113-3A= ENSP00000414946.2:n.2113-3A=
ENST00000562118.1:n.514-3A=
ENST00000562836.5:n.2367-3A=
ENST00000566510.5:c.*962-3A= ENSP00000458139.1:n.*962-3A=
ENST00000566612.5:c.*536-3A= ENSP00000454782.1:n.*536-3A=
ENST00000611625.4:c.2359-3A= ENSP00000481063.1:n.2359-3A=
ENST00000612417.4:c.1853+3097A= ENSP00000478360.1:n.1853+3097A=
ENST00000621016.4:c.1866-4552A= ENSP00000480664.1:n.1866-4552A=
NM_004360.3:c.2296-3A= , LRG_301t1:c.2296-3A= NP_004351.1:n.2296-3A=
XM_011523488.1:c.1561-3A= XP_011521790.1:n.1561-3A=
XM_011523489.1:c.1561-3A= XP_011521791.1:n.1561-3A=
NM_001317184.1:c.2113-3A= NP_001304113.1:n.2113-3A=
NM_001317185.1:c.748-3A= NP_001304114.1:n.748-3A=
NM_001317186.1:c.331-3A= NP_001304115.1:n.331-3A=
NM_004360.4:c.2296-3A= NP_004351.1:n.2296-3A=
NM_004360.5:c.2296-3A= MANE Select NP_004351.1:n.2296-3A=
NM_001317184.2:c.2113-3A= NP_001304113.1:n.2113-3A=
NM_001317185.2:c.748-3A= NP_001304114.1:n.748-3A=
NM_001317186.2:c.331-3A= NP_001304115.1:n.331-3A=