Canonical Allele Identifier: CA2229991875
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829632C= , CM000678.2:g.68829632C= GRCh38
NC_000016.9:g.68863535C= , CM000678.1:g.68863535C= GRCh37
NC_000016.8:g.67421036C= NCBI36
NG_008021.1:g.97341C= , LRG_301:g.97341C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2296-22C= MANE Select ENSP00000261769.4:n.2296-22C=
ENST00000261769.9:c.2296-22C= ENSP00000261769.4:n.2296-22C=
ENST00000422392.6:c.2113-22C= ENSP00000414946.2:n.2113-22C=
ENST00000562118.1:n.514-22C=
ENST00000562836.5:n.2367-22C=
ENST00000566510.5:c.*962-22C= ENSP00000458139.1:n.*962-22C=
ENST00000566612.5:c.*536-22C= ENSP00000454782.1:n.*536-22C=
ENST00000611625.4:c.2359-22C= ENSP00000481063.1:n.2359-22C=
ENST00000612417.4:c.1853+3078C= ENSP00000478360.1:n.1853+3078C=
ENST00000621016.4:c.1866-4571C= ENSP00000480664.1:n.1866-4571C=
NM_004360.3:c.2296-22C= , LRG_301t1:c.2296-22C= NP_004351.1:n.2296-22C=
XM_011523488.1:c.1561-22C= XP_011521790.1:n.1561-22C=
XM_011523489.1:c.1561-22C= XP_011521791.1:n.1561-22C=
NM_001317184.1:c.2113-22C= NP_001304113.1:n.2113-22C=
NM_001317185.1:c.748-22C= NP_001304114.1:n.748-22C=
NM_001317186.1:c.331-22C= NP_001304115.1:n.331-22C=
NM_004360.4:c.2296-22C= NP_004351.1:n.2296-22C=
NM_004360.5:c.2296-22C= MANE Select NP_004351.1:n.2296-22C=
NM_001317184.2:c.2113-22C= NP_001304113.1:n.2113-22C=
NM_001317185.2:c.748-22C= NP_001304114.1:n.748-22C=
NM_001317186.2:c.331-22C= NP_001304115.1:n.331-22C=