Canonical Allele Identifier: CA396457334
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs876660223

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801803G>T , CM000678.2:g.68801803G>T GRCh38
NC_000016.9:g.68835706G>T , CM000678.1:g.68835706G>T GRCh37
NC_000016.8:g.67393207G>T NCBI36
NG_008021.1:g.69512G>T , LRG_301:g.69512G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.297G>T MANE Select ENSP00000261769.4:p.Leu99Phe
ENST00000261769.9:c.297G>T ENSP00000261769.4:p.Leu99Phe
ENST00000422392.6:c.297G>T ENSP00000414946.2:p.Leu99Phe
ENST00000561751.1:c.64G>T
ENST00000562836.5:n.368G>T
ENST00000564676.5:n.579G>T
ENST00000564745.1:n.292G>T
ENST00000566510.5:c.297G>T ENSP00000458139.1:p.Leu99Phe
ENST00000566612.5:c.297G>T ENSP00000454782.1:p.Leu99Phe
ENST00000611625.4:c.297G>T ENSP00000481063.1:p.Leu99Phe
ENST00000612417.4:c.297G>T ENSP00000478360.1:p.Leu99Phe
ENST00000621016.4:c.297G>T ENSP00000480664.1:p.Leu99Phe
NM_004360.3:c.297G>T , LRG_301t1:c.297G>T NP_004351.1:p.Leu99Phe
XM_011523488.1:c.-439G>T XP_011521790.1:n.-439G>T
XM_011523489.1:c.-439G>T XP_011521791.1:n.-439G>T
NM_001317184.1:c.297G>T NP_001304113.1:p.Leu99Phe
NM_001317185.1:c.-1319G>T NP_001304114.1:n.-1319G>T
NM_001317186.1:c.-1523G>T NP_001304115.1:n.-1523G>T
NM_004360.4:c.297G>T NP_004351.1:p.Leu99Phe
NM_004360.5:c.297G>T MANE Select NP_004351.1:p.Leu99Phe
NM_001317184.2:c.297G>T NP_001304113.1:p.Leu99Phe
NM_001317185.2:c.-1319G>T NP_001304114.1:n.-1319G>T
NM_001317186.2:c.-1523G>T NP_001304115.1:n.-1523G>T