Canonical Allele Identifier: CA2807472326
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810565_68810566insT , CM000678.2:g.68810565_68810566insT GRCh38
NC_000016.9:g.68844468_68844469insT , CM000678.1:g.68844468_68844469insT GRCh37
NC_000016.8:g.67401969_67401970insT NCBI36
NG_008021.1:g.78274_78275insT , LRG_301:g.78274_78275insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.832+224_832+225insT MANE Select ENSP00000261769.4:n.832+224_832+225insT
ENST00000261769.9:c.832+224_832+225insT ENSP00000261769.4:n.832+224_832+225insT
ENST00000422392.6:c.832+224_832+225insT ENSP00000414946.2:n.832+224_832+225insT
ENST00000561751.1:c.455-1119_455-1118insT
ENST00000562836.5:n.903+224_903+225insT
ENST00000566510.5:c.676+224_676+225insT ENSP00000458139.1:n.676+224_676+225insT
ENST00000566612.5:c.832+224_832+225insT ENSP00000454782.1:n.832+224_832+225insT
ENST00000611625.4:c.832+224_832+225insT ENSP00000481063.1:n.832+224_832+225insT
ENST00000612417.4:c.832+224_832+225insT ENSP00000478360.1:n.832+224_832+225insT
ENST00000621016.4:c.832+224_832+225insT ENSP00000480664.1:n.832+224_832+225insT
NM_004360.3:c.832+224_832+225insT , LRG_301t1:c.832+224_832+225insT NP_004351.1:n.832+224_832+225insT
XM_011523488.1:c.97+224_97+225insT XP_011521790.1:n.97+224_97+225insT
XM_011523489.1:c.97+224_97+225insT XP_011521791.1:n.97+224_97+225insT
NM_001317184.1:c.832+224_832+225insT NP_001304113.1:n.832+224_832+225insT
NM_001317185.1:c.-784+224_-784+225insT NP_001304114.1:n.-784+224_-784+225insT
NM_001317186.1:c.-988+224_-988+225insT NP_001304115.1:n.-988+224_-988+225insT
NM_004360.4:c.832+224_832+225insT NP_004351.1:n.832+224_832+225insT
NM_004360.5:c.832+224_832+225insT MANE Select NP_004351.1:n.832+224_832+225insT
NM_001317184.2:c.832+224_832+225insT NP_001304113.1:n.832+224_832+225insT
NM_001317185.2:c.-784+224_-784+225insT NP_001304114.1:n.-784+224_-784+225insT
NM_001317186.2:c.-988+224_-988+225insT NP_001304115.1:n.-988+224_-988+225insT