Canonical Allele Identifier: CA396459936
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs116093741

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68812144A>C , CM000678.2:g.68812144A>C GRCh38
NC_000016.9:g.68846047A>C , CM000678.1:g.68846047A>C GRCh37
NC_000016.8:g.67403548A>C NCBI36
NG_008021.1:g.79853A>C , LRG_301:g.79853A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1018A>C MANE Select ENSP00000261769.4:p.Thr340Pro
ENST00000261769.9:c.1018A>C ENSP00000261769.4:p.Thr340Pro
ENST00000422392.6:c.1018A>C ENSP00000414946.2:p.Thr340Pro
ENST00000561751.1:c.640A>C
ENST00000562836.5:n.1089A>C
ENST00000565810.1:n.62A>C
ENST00000566510.5:c.862A>C ENSP00000458139.1:p.Thr288Pro
ENST00000566612.5:c.1018A>C ENSP00000454782.1:p.Thr340Pro
ENST00000611625.4:c.1018A>C ENSP00000481063.1:p.Thr340Pro
ENST00000612417.4:c.1018A>C ENSP00000478360.1:p.Thr340Pro
ENST00000621016.4:c.1018A>C ENSP00000480664.1:p.Thr340Pro
NM_004360.3:c.1018A>C , LRG_301t1:c.1018A>C NP_004351.1:p.Thr340Pro
XM_011523488.1:c.283A>C XP_011521790.1:p.Thr95Pro
XM_011523489.1:c.283A>C XP_011521791.1:p.Thr95Pro
NM_001317184.1:c.1018A>C NP_001304113.1:p.Thr340Pro
NM_001317185.1:c.-598A>C NP_001304114.1:n.-598A>C
NM_001317186.1:c.-802A>C NP_001304115.1:n.-802A>C
NM_004360.4:c.1018A>C NP_004351.1:p.Thr340Pro
NM_004360.5:c.1018A>C MANE Select NP_004351.1:p.Thr340Pro
NM_001317184.2:c.1018A>C NP_001304113.1:p.Thr340Pro
NM_001317185.2:c.-598A>C NP_001304114.1:n.-598A>C
NM_001317186.2:c.-802A>C NP_001304115.1:n.-802A>C