Canonical Allele Identifier: CA2633931820
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819556_68819557insC , CM000678.2:g.68819556_68819557insC GRCh38
NC_000016.9:g.68853459_68853460insC , CM000678.1:g.68853459_68853460insC GRCh37
NC_000016.8:g.67410960_67410961insC NCBI36
NG_008021.1:g.87265_87266insC , LRG_301:g.87265_87266insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1711+131_1711+132insC MANE Select ENSP00000261769.4:n.1711+131_1711+132insC
ENST00000261769.9:c.1711+131_1711+132insC ENSP00000261769.4:n.1711+131_1711+132insC
ENST00000422392.6:c.1528+131_1528+132insC ENSP00000414946.2:n.1528+131_1528+132insC
ENST00000562836.5:n.1782+131_1782+132insC
ENST00000566510.5:c.*377+131_*377+132insC ENSP00000458139.1:n.*377+131_*377+132insC
ENST00000566612.5:c.1566-2445_1566-2444insC ENSP00000454782.1:n.1566-2445_1566-2444insC
ENST00000611625.4:c.1774+131_1774+132insC ENSP00000481063.1:n.1774+131_1774+132insC
ENST00000612417.4:c.1711+131_1711+132insC ENSP00000478360.1:n.1711+131_1711+132insC
ENST00000621016.4:c.1711+131_1711+132insC ENSP00000480664.1:n.1711+131_1711+132insC
NM_004360.3:c.1711+131_1711+132insC , LRG_301t1:c.1711+131_1711+132insC NP_004351.1:n.1711+131_1711+132insC
XM_011523488.1:c.976+131_976+132insC XP_011521790.1:n.976+131_976+132insC
XM_011523489.1:c.976+131_976+132insC XP_011521791.1:n.976+131_976+132insC
NM_001317184.1:c.1528+131_1528+132insC NP_001304113.1:n.1528+131_1528+132insC
NM_001317185.1:c.163+131_163+132insC NP_001304114.1:n.163+131_163+132insC
NM_001317186.1:c.-254-2445_-254-2444insC NP_001304115.1:n.-254-2445_-254-2444insC
NM_004360.4:c.1711+131_1711+132insC NP_004351.1:n.1711+131_1711+132insC
NM_004360.5:c.1711+131_1711+132insC MANE Select NP_004351.1:n.1711+131_1711+132insC
NM_001317184.2:c.1528+131_1528+132insC NP_001304113.1:n.1528+131_1528+132insC
NM_001317185.2:c.163+131_163+132insC NP_001304114.1:n.163+131_163+132insC
NM_001317186.2:c.-254-2445_-254-2444insC NP_001304115.1:n.-254-2445_-254-2444insC