Canonical Allele Identifier: CA2229991755
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829559A= , CM000678.2:g.68829559A= GRCh38
NC_000016.9:g.68863462A= , CM000678.1:g.68863462A= GRCh37
NC_000016.8:g.67420963A= NCBI36
NG_008021.1:g.97268A= , LRG_301:g.97268A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2296-95A= MANE Select ENSP00000261769.4:n.2296-95A=
ENST00000261769.9:c.2296-95A= ENSP00000261769.4:n.2296-95A=
ENST00000422392.6:c.2113-95A= ENSP00000414946.2:n.2113-95A=
ENST00000562118.1:n.514-95A=
ENST00000562836.5:n.2367-95A=
ENST00000566510.5:c.*962-95A= ENSP00000458139.1:n.*962-95A=
ENST00000566612.5:c.*536-95A= ENSP00000454782.1:n.*536-95A=
ENST00000611625.4:c.2359-95A= ENSP00000481063.1:n.2359-95A=
ENST00000612417.4:c.1853+3005A= ENSP00000478360.1:n.1853+3005A=
ENST00000621016.4:c.1866-4644A= ENSP00000480664.1:n.1866-4644A=
NM_004360.3:c.2296-95A= , LRG_301t1:c.2296-95A= NP_004351.1:n.2296-95A=
XM_011523488.1:c.1561-95A= XP_011521790.1:n.1561-95A=
XM_011523489.1:c.1561-95A= XP_011521791.1:n.1561-95A=
NM_001317184.1:c.2113-95A= NP_001304113.1:n.2113-95A=
NM_001317185.1:c.748-95A= NP_001304114.1:n.748-95A=
NM_001317186.1:c.331-95A= NP_001304115.1:n.331-95A=
NM_004360.4:c.2296-95A= NP_004351.1:n.2296-95A=
NM_004360.5:c.2296-95A= MANE Select NP_004351.1:n.2296-95A=
NM_001317184.2:c.2113-95A= NP_001304113.1:n.2113-95A=
NM_001317185.2:c.748-95A= NP_001304114.1:n.748-95A=
NM_001317186.2:c.331-95A= NP_001304115.1:n.331-95A=