Canonical Allele Identifier: CA623137050
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1479302039

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68818867_68818868insG , CM000678.2:g.68818867_68818868insG GRCh38
NC_000016.9:g.68852770_68852771insG , CM000678.1:g.68852770_68852771insG GRCh37
NC_000016.8:g.67410271_67410272insG NCBI36
NG_008021.1:g.86576_86577insG , LRG_301:g.86576_86577insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1566-413_1566-412insG MANE Select ENSP00000261769.4:n.1566-413_1566-412insG
ENST00000261769.9:c.1566-413_1566-412insG ENSP00000261769.4:n.1566-413_1566-412insG
ENST00000422392.6:c.1383-413_1383-412insG ENSP00000414946.2:n.1383-413_1383-412insG
ENST00000562836.5:n.1637-413_1637-412insG
ENST00000566510.5:c.*232-413_*232-412insG ENSP00000458139.1:n.*232-413_*232-412insG
ENST00000566612.5:c.1565+3108_1565+3109insG ENSP00000454782.1:n.1565+3108_1565+3109insG
ENST00000611625.4:c.1629-413_1629-412insG ENSP00000481063.1:n.1629-413_1629-412insG
ENST00000612417.4:c.1566-413_1566-412insG ENSP00000478360.1:n.1566-413_1566-412insG
ENST00000621016.4:c.1566-413_1566-412insG ENSP00000480664.1:n.1566-413_1566-412insG
NM_004360.3:c.1566-413_1566-412insG , LRG_301t1:c.1566-413_1566-412insG NP_004351.1:n.1566-413_1566-412insG
XM_011523488.1:c.831-413_831-412insG XP_011521790.1:n.831-413_831-412insG
XM_011523489.1:c.831-413_831-412insG XP_011521791.1:n.831-413_831-412insG
NM_001317184.1:c.1383-413_1383-412insG NP_001304113.1:n.1383-413_1383-412insG
NM_001317185.1:c.18-413_18-412insG NP_001304114.1:n.18-413_18-412insG
NM_001317186.1:c.-255+3108_-255+3109insG NP_001304115.1:n.-255+3108_-255+3109insG
NM_004360.4:c.1566-413_1566-412insG NP_004351.1:n.1566-413_1566-412insG
NM_004360.5:c.1566-413_1566-412insG MANE Select NP_004351.1:n.1566-413_1566-412insG
NM_001317184.2:c.1383-413_1383-412insG NP_001304113.1:n.1383-413_1383-412insG
NM_001317185.2:c.18-413_18-412insG NP_001304114.1:n.18-413_18-412insG
NM_001317186.2:c.-255+3108_-255+3109insG NP_001304115.1:n.-255+3108_-255+3109insG