Canonical Allele Identifier: CA2229967568
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1960793887

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810570_68810571insA , CM000678.2:g.68810570_68810571insA GRCh38
NC_000016.9:g.68844473_68844474insA , CM000678.1:g.68844473_68844474insA GRCh37
NC_000016.8:g.67401974_67401975insA NCBI36
NG_008021.1:g.78279_78280insA , LRG_301:g.78279_78280insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.832+229_832+230insA MANE Select ENSP00000261769.4:n.832+229_832+230insA
ENST00000261769.9:c.832+229_832+230insA ENSP00000261769.4:n.832+229_832+230insA
ENST00000422392.6:c.832+229_832+230insA ENSP00000414946.2:n.832+229_832+230insA
ENST00000561751.1:c.455-1114_455-1113insA
ENST00000562836.5:n.903+229_903+230insA
ENST00000566510.5:c.676+229_676+230insA ENSP00000458139.1:n.676+229_676+230insA
ENST00000566612.5:c.832+229_832+230insA ENSP00000454782.1:n.832+229_832+230insA
ENST00000611625.4:c.832+229_832+230insA ENSP00000481063.1:n.832+229_832+230insA
ENST00000612417.4:c.832+229_832+230insA ENSP00000478360.1:n.832+229_832+230insA
ENST00000621016.4:c.832+229_832+230insA ENSP00000480664.1:n.832+229_832+230insA
NM_004360.3:c.832+229_832+230insA , LRG_301t1:c.832+229_832+230insA NP_004351.1:n.832+229_832+230insA
XM_011523488.1:c.97+229_97+230insA XP_011521790.1:n.97+229_97+230insA
XM_011523489.1:c.97+229_97+230insA XP_011521791.1:n.97+229_97+230insA
NM_001317184.1:c.832+229_832+230insA NP_001304113.1:n.832+229_832+230insA
NM_001317185.1:c.-784+229_-784+230insA NP_001304114.1:n.-784+229_-784+230insA
NM_001317186.1:c.-988+229_-988+230insA NP_001304115.1:n.-988+229_-988+230insA
NM_004360.4:c.832+229_832+230insA NP_004351.1:n.832+229_832+230insA
NM_004360.5:c.832+229_832+230insA MANE Select NP_004351.1:n.832+229_832+230insA
NM_001317184.2:c.832+229_832+230insA NP_001304113.1:n.832+229_832+230insA
NM_001317185.2:c.-784+229_-784+230insA NP_001304114.1:n.-784+229_-784+230insA
NM_001317186.2:c.-988+229_-988+230insA NP_001304115.1:n.-988+229_-988+230insA