Canonical Allele Identifier: CA2229977198
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1961058795

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68818866_68818867insG , CM000678.2:g.68818866_68818867insG GRCh38
NC_000016.9:g.68852769_68852770insG , CM000678.1:g.68852769_68852770insG GRCh37
NC_000016.8:g.67410270_67410271insG NCBI36
NG_008021.1:g.86575_86576insG , LRG_301:g.86575_86576insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1566-414_1566-413insG MANE Select ENSP00000261769.4:n.1566-414_1566-413insG
ENST00000261769.9:c.1566-414_1566-413insG ENSP00000261769.4:n.1566-414_1566-413insG
ENST00000422392.6:c.1383-414_1383-413insG ENSP00000414946.2:n.1383-414_1383-413insG
ENST00000562836.5:n.1637-414_1637-413insG
ENST00000566510.5:c.*232-414_*232-413insG ENSP00000458139.1:n.*232-414_*232-413insG
ENST00000566612.5:c.1565+3107_1565+3108insG ENSP00000454782.1:n.1565+3107_1565+3108insG
ENST00000611625.4:c.1629-414_1629-413insG ENSP00000481063.1:n.1629-414_1629-413insG
ENST00000612417.4:c.1566-414_1566-413insG ENSP00000478360.1:n.1566-414_1566-413insG
ENST00000621016.4:c.1566-414_1566-413insG ENSP00000480664.1:n.1566-414_1566-413insG
NM_004360.3:c.1566-414_1566-413insG , LRG_301t1:c.1566-414_1566-413insG NP_004351.1:n.1566-414_1566-413insG
XM_011523488.1:c.831-414_831-413insG XP_011521790.1:n.831-414_831-413insG
XM_011523489.1:c.831-414_831-413insG XP_011521791.1:n.831-414_831-413insG
NM_001317184.1:c.1383-414_1383-413insG NP_001304113.1:n.1383-414_1383-413insG
NM_001317185.1:c.18-414_18-413insG NP_001304114.1:n.18-414_18-413insG
NM_001317186.1:c.-255+3107_-255+3108insG NP_001304115.1:n.-255+3107_-255+3108insG
NM_004360.4:c.1566-414_1566-413insG NP_004351.1:n.1566-414_1566-413insG
NM_004360.5:c.1566-414_1566-413insG MANE Select NP_004351.1:n.1566-414_1566-413insG
NM_001317184.2:c.1383-414_1383-413insG NP_001304113.1:n.1383-414_1383-413insG
NM_001317185.2:c.18-414_18-413insG NP_001304114.1:n.18-414_18-413insG
NM_001317186.2:c.-255+3107_-255+3108insG NP_001304115.1:n.-255+3107_-255+3108insG