Canonical Allele Identifier: CA2633897557
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1962418276

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737346C>A , CM000678.2:g.68737346C>A GRCh38
NC_000016.9:g.68771249C>A , CM000678.1:g.68771249C>A GRCh37
NC_000016.8:g.67328750C>A NCBI36
NG_008021.1:g.5055C>A , LRG_301:g.5055C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.-70C>A MANE Select ENSP00000261769.4:n.-70C>A
ENST00000261769.9:c.-70C>A ENSP00000261769.4:n.-70C>A
ENST00000566612.5:c.-70C>A ENSP00000454782.1:n.-70C>A
ENST00000611625.4:c.-70C>A ENSP00000481063.1:n.-70C>A
ENST00000612417.4:c.-70C>A ENSP00000478360.1:n.-70C>A
ENST00000621016.4:c.-70C>A ENSP00000480664.1:n.-70C>A
NM_004360.3:c.-70C>A , LRG_301t1:c.-70C>A NP_004351.1:n.-70C>A
NM_001317184.1:c.-70C>A NP_001304113.1:n.-70C>A
NM_001317185.1:c.-1685C>A NP_001304114.1:n.-1685C>A
NM_001317186.1:c.-1889C>A NP_001304115.1:n.-1889C>A
NM_004360.4:c.-70C>A NP_004351.1:n.-70C>A
NM_004360.5:c.-70C>A MANE Select NP_004351.1:n.-70C>A
NM_001317184.2:c.-70C>A NP_001304113.1:n.-70C>A
NM_001317185.2:c.-1685C>A NP_001304114.1:n.-1685C>A
NM_001317186.2:c.-1889C>A NP_001304115.1:n.-1889C>A