Canonical Allele Identifier: CA2633932065
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829921C>A , CM000678.2:g.68829921C>A GRCh38
NC_000016.9:g.68863824C>A , CM000678.1:g.68863824C>A GRCh37
NC_000016.8:g.67421325C>A NCBI36
NG_008021.1:g.97630C>A , LRG_301:g.97630C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+124C>A MANE Select ENSP00000261769.4:n.2439+124C>A
ENST00000261769.9:c.2439+124C>A ENSP00000261769.4:n.2439+124C>A
ENST00000422392.6:c.2256+124C>A ENSP00000414946.2:n.2256+124C>A
ENST00000562118.1:n.657+124C>A
ENST00000562836.5:n.2510+124C>A
ENST00000566510.5:c.*1105+124C>A ENSP00000458139.1:n.*1105+124C>A
ENST00000566612.5:c.*679+124C>A ENSP00000454782.1:n.*679+124C>A
ENST00000611625.4:c.2502+124C>A ENSP00000481063.1:n.2502+124C>A
ENST00000612417.4:c.1853+3367C>A ENSP00000478360.1:n.1853+3367C>A
ENST00000621016.4:c.1866-4282C>A ENSP00000480664.1:n.1866-4282C>A
NM_004360.3:c.2439+124C>A , LRG_301t1:c.2439+124C>A NP_004351.1:n.2439+124C>A
XM_011523488.1:c.1704+124C>A XP_011521790.1:n.1704+124C>A
XM_011523489.1:c.1704+124C>A XP_011521791.1:n.1704+124C>A
NM_001317184.1:c.2256+124C>A NP_001304113.1:n.2256+124C>A
NM_001317185.1:c.891+124C>A NP_001304114.1:n.891+124C>A
NM_001317186.1:c.474+124C>A NP_001304115.1:n.474+124C>A
NM_004360.4:c.2439+124C>A NP_004351.1:n.2439+124C>A
NM_004360.5:c.2439+124C>A MANE Select NP_004351.1:n.2439+124C>A
NM_001317184.2:c.2256+124C>A NP_001304113.1:n.2256+124C>A
NM_001317185.2:c.891+124C>A NP_001304114.1:n.891+124C>A
NM_001317186.2:c.474+124C>A NP_001304115.1:n.474+124C>A