Canonical Allele Identifier: CA2229977981
Gene: CDH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819324_68819325delinsCG , CM000678.2:g.68819324_68819325delinsCG GRCh38
NC_000016.9:g.68853227_68853228delinsCG , CM000678.1:g.68853227_68853228delinsCG GRCh37
NC_000016.8:g.67410728_67410729delinsCG NCBI36
NG_008021.1:g.87033_87034delinsCG , LRG_301:g.87033_87034delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1610_1611delinsCG MANE Select ENSP00000261769.4:p.Pro537=
ENST00000261769.9:c.1610_1611delinsCG ENSP00000261769.4:p.Pro537=
ENST00000422392.6:c.1427_1428delinsCG ENSP00000414946.2:p.Pro476=
ENST00000562836.5:n.1681_1682delinsCG
ENST00000566510.5:c.*276_*277delinsCG ENSP00000458139.1:n.*276_*277delinsCG
ENST00000566612.5:c.1566-2677_1566-2676delinsCG ENSP00000454782.1:n.1566-2677_1566-2676delinsCG
ENST00000611625.4:c.1673_1674delinsCG ENSP00000481063.1:p.Pro558=
ENST00000612417.4:c.1610_1611delinsCG ENSP00000478360.1:p.Pro537=
ENST00000621016.4:c.1610_1611delinsCG ENSP00000480664.1:p.Pro537=
NM_004360.3:c.1610_1611delinsCG , LRG_301t1:c.1610_1611delinsCG NP_004351.1:p.Pro537=
XM_011523488.1:c.875_876delinsCG XP_011521790.1:p.Pro292=
XM_011523489.1:c.875_876delinsCG XP_011521791.1:p.Pro292=
NM_001317184.1:c.1427_1428delinsCG NP_001304113.1:p.Pro476=
NM_001317185.1:c.62_63delinsCG NP_001304114.1:p.Pro21=
NM_001317186.1:c.-254-2677_-254-2676delinsCG NP_001304115.1:n.-254-2677_-254-2676delinsCG
NM_004360.4:c.1610_1611delinsCG NP_004351.1:p.Pro537=
NM_004360.5:c.1610_1611delinsCG MANE Select NP_004351.1:p.Pro537=
NM_001317184.2:c.1427_1428delinsCG NP_001304113.1:p.Pro476=
NM_001317185.2:c.62_63delinsCG NP_001304114.1:p.Pro21=
NM_001317186.2:c.-254-2677_-254-2676delinsCG NP_001304115.1:n.-254-2677_-254-2676delinsCG
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