Canonical Allele Identifier: CA2633898719
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737514_68737515insAG , CM000678.2:g.68737514_68737515insAG GRCh38
NC_000016.9:g.68771417_68771418insAG , CM000678.1:g.68771417_68771418insAG GRCh37
NC_000016.8:g.67328918_67328919insAG NCBI36
NG_008021.1:g.5223_5224insAG , LRG_301:g.5223_5224insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.48+51_48+52insAG MANE Select ENSP00000261769.4:n.48+51_48+52insAG
ENST00000261769.9:c.48+51_48+52insAG ENSP00000261769.4:n.48+51_48+52insAG
ENST00000422392.6:c.48+51_48+52insAG ENSP00000414946.2:n.48+51_48+52insAG
ENST00000566510.5:c.48+51_48+52insAG ENSP00000458139.1:n.48+51_48+52insAG
ENST00000566612.5:c.48+51_48+52insAG ENSP00000454782.1:n.48+51_48+52insAG
ENST00000611625.4:c.48+51_48+52insAG ENSP00000481063.1:n.48+51_48+52insAG
ENST00000612417.4:c.48+51_48+52insAG ENSP00000478360.1:n.48+51_48+52insAG
ENST00000621016.4:c.48+51_48+52insAG ENSP00000480664.1:n.48+51_48+52insAG
NM_004360.3:c.48+51_48+52insAG , LRG_301t1:c.48+51_48+52insAG NP_004351.1:n.48+51_48+52insAG
NM_001317184.1:c.48+51_48+52insAG NP_001304113.1:n.48+51_48+52insAG
NM_001317185.1:c.-1568+51_-1568+52insAG NP_001304114.1:n.-1568+51_-1568+52insAG
NM_001317186.1:c.-1772+51_-1772+52insAG NP_001304115.1:n.-1772+51_-1772+52insAG
NM_004360.4:c.48+51_48+52insAG NP_004351.1:n.48+51_48+52insAG
NM_004360.5:c.48+51_48+52insAG MANE Select NP_004351.1:n.48+51_48+52insAG
NM_001317184.2:c.48+51_48+52insAG NP_001304113.1:n.48+51_48+52insAG
NM_001317185.2:c.-1568+51_-1568+52insAG NP_001304114.1:n.-1568+51_-1568+52insAG
NM_001317186.2:c.-1772+51_-1772+52insAG NP_001304115.1:n.-1772+51_-1772+52insAG