Canonical Allele Identifier: CA891842216
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833402_68833403del , CM000678.2:g.68833402_68833403del GRCh38
NC_000016.9:g.68867305_68867306del , CM000678.1:g.68867305_68867306del GRCh37
NC_000016.8:g.67424806_67424807del NCBI36
NG_008021.1:g.101111_101112del , LRG_301:g.101111_101112del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2552_2553del MANE Select ENSP00000261769.4:p.Ser851Ter
ENST00000261769.9:c.2552_2553del ENSP00000261769.4:p.Ser851Ter
ENST00000422392.6:c.2369_2370del ENSP00000414946.2:p.Ser790Ter
ENST00000562118.1:n.770_771del
ENST00000562836.5:n.2623_2624del
ENST00000566510.5:c.*1218_*1219del ENSP00000458139.1:n.*1218_*1219del
ENST00000566612.5:c.*792_*793del ENSP00000454782.1:n.*792_*793del
ENST00000611625.4:c.2615_2616del ENSP00000481063.1:p.Ser872Ter
ENST00000612417.4:c.1854-789_1854-788del ENSP00000478360.1:n.1854-789_1854-788del
ENST00000621016.4:c.1866-801_1866-800del ENSP00000480664.1:n.1866-801_1866-800del
NM_004360.3:c.2552_2553del , LRG_301t1:c.2552_2553del NP_004351.1:p.Ser851Ter
XM_011523488.1:c.1817_1818del XP_011521790.1:p.Ser606Ter
XM_011523489.1:c.1817_1818del XP_011521791.1:p.Ser606Ter
NM_001317184.1:c.2369_2370del NP_001304113.1:p.Ser790Ter
NM_001317185.1:c.1004_1005del NP_001304114.1:p.Ser335Ter
NM_001317186.1:c.587_588del NP_001304115.1:p.Ser196Ter
NM_004360.4:c.2552_2553del NP_004351.1:p.Ser851Ter
NM_004360.5:c.2552_2553del MANE Select NP_004351.1:p.Ser851Ter
NM_001317184.2:c.2369_2370del NP_001304113.1:p.Ser790Ter
NM_001317185.2:c.1004_1005del NP_001304114.1:p.Ser335Ter
NM_001317186.2:c.587_588del NP_001304115.1:p.Ser196Ter