Canonical Allele Identifier: CA2576038569
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737395dup , CM000678.2:g.68737395dup GRCh38
NC_000016.9:g.68771298dup , CM000678.1:g.68771298dup GRCh37
NC_000016.8:g.67328799dup NCBI36
NG_008021.1:g.5104dup , LRG_301:g.5104dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.-21dup MANE Select ENSP00000261769.4:n.-21dup
ENST00000261769.9:c.-21dup ENSP00000261769.4:n.-21dup
ENST00000422392.6:c.-21dup ENSP00000414946.2:n.-21dup
ENST00000566510.5:c.-21dup ENSP00000458139.1:n.-21dup
ENST00000566612.5:c.-21dup ENSP00000454782.1:n.-21dup
ENST00000611625.4:c.-21dup ENSP00000481063.1:n.-21dup
ENST00000612417.4:c.-21dup ENSP00000478360.1:n.-21dup
ENST00000621016.4:c.-21dup ENSP00000480664.1:n.-21dup
NM_004360.3:c.-21dup , LRG_301t1:c.-21dup NP_004351.1:n.-21dup
NM_001317184.1:c.-21dup NP_001304113.1:n.-21dup
NM_001317185.1:c.-1636dup NP_001304114.1:n.-1636dup
NM_001317186.1:c.-1840dup NP_001304115.1:n.-1840dup
NM_004360.4:c.-21dup NP_004351.1:n.-21dup
NM_004360.5:c.-21dup MANE Select NP_004351.1:n.-21dup
NM_001317184.2:c.-21dup NP_001304113.1:n.-21dup
NM_001317185.2:c.-1636dup NP_001304114.1:n.-1636dup
NM_001317186.2:c.-1840dup NP_001304115.1:n.-1840dup