Canonical Allele Identifier: CA2229975082
Gene: CDH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829752_68829753delinsTC , CM000678.2:g.68829752_68829753delinsTC GRCh38
NC_000016.9:g.68863655_68863656delinsTC , CM000678.1:g.68863655_68863656delinsTC GRCh37
NC_000016.8:g.67421156_67421157delinsTC NCBI36
NG_008021.1:g.97461_97462delinsTC , LRG_301:g.97461_97462delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2394_2395delinsTC MANE Select ENSP00000261769.4:p.Leu798=
ENST00000261769.9:c.2394_2395delinsTC ENSP00000261769.4:p.Leu798=
ENST00000422392.6:c.2211_2212delinsTC ENSP00000414946.2:p.Leu737=
ENST00000562118.1:n.612_613delinsTC
ENST00000562836.5:n.2465_2466delinsTC
ENST00000566510.5:c.*1060_*1061delinsTC ENSP00000458139.1:n.*1060_*1061delinsTC
ENST00000566612.5:c.*634_*635delinsTC ENSP00000454782.1:n.*634_*635delinsTC
ENST00000611625.4:c.2457_2458delinsTC ENSP00000481063.1:p.Leu819=
ENST00000612417.4:c.1853+3198_1853+3199delinsTC ENSP00000478360.1:n.1853+3198_1853+3199delinsTC
ENST00000621016.4:c.1866-4451_1866-4450delinsTC ENSP00000480664.1:n.1866-4451_1866-4450delinsTC
NM_004360.3:c.2394_2395delinsTC , LRG_301t1:c.2394_2395delinsTC NP_004351.1:p.Leu798=
XM_011523488.1:c.1659_1660delinsTC XP_011521790.1:p.Leu553=
XM_011523489.1:c.1659_1660delinsTC XP_011521791.1:p.Leu553=
NM_001317184.1:c.2211_2212delinsTC NP_001304113.1:p.Leu737=
NM_001317185.1:c.846_847delinsTC NP_001304114.1:p.Leu282=
NM_001317186.1:c.429_430delinsTC NP_001304115.1:p.Leu143=
NM_004360.4:c.2394_2395delinsTC NP_004351.1:p.Leu798=
NM_004360.5:c.2394_2395delinsTC MANE Select NP_004351.1:p.Leu798=
NM_001317184.2:c.2211_2212delinsTC NP_001304113.1:p.Leu737=
NM_001317185.2:c.846_847delinsTC NP_001304114.1:p.Leu282=
NM_001317186.2:c.429_430delinsTC NP_001304115.1:p.Leu143=
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