Canonical Allele Identifier: CA2229953337
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68796624_68796637delinsTCTCTCTTGGGGTC , CM000678.2:g.68796624_68796637delinsTCTCTCTTGGGGTC GRCh38
NC_000016.9:g.68830527_68830540delinsTCTCTCTTGGGGTC , CM000678.1:g.68830527_68830540delinsTCTCTCTTGGGGTC GRCh37
NC_000016.8:g.67388028_67388041delinsTCTCTCTTGGGGTC NCBI36
NG_008021.1:g.64333_64346delinsTCTCTCTTGGGGTC , LRG_301:g.64333_64346delinsTCTCTCTTGGGGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.164-5046_164-5033delinsTCTCTCTTGGGGTC MANE Select ENSP00000261769.4:n.164-5046_164-5033delinsTCTCTCTTGGGGTC
ENST00000261769.9:c.164-5046_164-5033delinsTCTCTCTTGGGGTC ENSP00000261769.4:n.164-5046_164-5033delinsTCTCTCTTGGGGTC
ENST00000422392.6:c.164-5046_164-5033delinsTCTCTCTTGGGGTC ENSP00000414946.2:n.164-5046_164-5033delinsTCTCTCTTGGGGTC
ENST00000562836.5:n.235-5046_235-5033delinsTCTCTCTTGGGGTC
ENST00000564676.5:n.446-5046_446-5033delinsTCTCTCTTGGGGTC
ENST00000564745.1:n.159-5046_159-5033delinsTCTCTCTTGGGGTC
ENST00000566510.5:c.164-5046_164-5033delinsTCTCTCTTGGGGTC ENSP00000458139.1:n.164-5046_164-5033delinsTCTCTCTTGGGGTC
ENST00000566612.5:c.164-5046_164-5033delinsTCTCTCTTGGGGTC ENSP00000454782.1:n.164-5046_164-5033delinsTCTCTCTTGGGGTC
ENST00000611625.4:c.164-5046_164-5033delinsTCTCTCTTGGGGTC ENSP00000481063.1:n.164-5046_164-5033delinsTCTCTCTTGGGGTC
ENST00000612417.4:c.164-5046_164-5033delinsTCTCTCTTGGGGTC ENSP00000478360.1:n.164-5046_164-5033delinsTCTCTCTTGGGGTC
ENST00000621016.4:c.164-5046_164-5033delinsTCTCTCTTGGGGTC ENSP00000480664.1:n.164-5046_164-5033delinsTCTCTCTTGGGGTC
NM_004360.3:c.164-5046_164-5033delinsTCTCTCTTGGGGTC , LRG_301t1:c.164-5046_164-5033delinsTCTCTCTTGGGGTC NP_004351.1:n.164-5046_164-5033delinsTCTCTCTTGGGGTC
XM_011523488.1:c.-572-5046_-572-5033delinsTCTCTCTTGGGGTC XP_011521790.1:n.-572-5046_-572-5033delinsTCTCTCTTGGGGTC
XM_011523489.1:c.-572-5046_-572-5033delinsTCTCTCTTGGGGTC XP_011521791.1:n.-572-5046_-572-5033delinsTCTCTCTTGGGGTC
NM_001317184.1:c.164-5046_164-5033delinsTCTCTCTTGGGGTC NP_001304113.1:n.164-5046_164-5033delinsTCTCTCTTGGGGTC
NM_001317185.1:c.-1452-5046_-1452-5033delinsTCTCTCTTGGGGTC NP_001304114.1:n.-1452-5046_-1452-5033delinsTCTCTCTTGGGGTC
NM_001317186.1:c.-1656-5046_-1656-5033delinsTCTCTCTTGGGGTC NP_001304115.1:n.-1656-5046_-1656-5033delinsTCTCTCTTGGGGTC
NM_004360.4:c.164-5046_164-5033delinsTCTCTCTTGGGGTC NP_004351.1:n.164-5046_164-5033delinsTCTCTCTTGGGGTC
NM_004360.5:c.164-5046_164-5033delinsTCTCTCTTGGGGTC MANE Select NP_004351.1:n.164-5046_164-5033delinsTCTCTCTTGGGGTC
NM_001317184.2:c.164-5046_164-5033delinsTCTCTCTTGGGGTC NP_001304113.1:n.164-5046_164-5033delinsTCTCTCTTGGGGTC
NM_001317185.2:c.-1452-5046_-1452-5033delinsTCTCTCTTGGGGTC NP_001304114.1:n.-1452-5046_-1452-5033delinsTCTCTCTTGGGGTC
NM_001317186.2:c.-1656-5046_-1656-5033delinsTCTCTCTTGGGGTC NP_001304115.1:n.-1656-5046_-1656-5033delinsTCTCTCTTGGGGTC