Canonical Allele Identifier: CA2576038985
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833594T>C , CM000678.2:g.68833594T>C GRCh38
NC_000016.9:g.68867497T>C , CM000678.1:g.68867497T>C GRCh37
NC_000016.8:g.67424998T>C NCBI36
NG_008021.1:g.101303T>C , LRG_301:g.101303T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.*95T>C MANE Select ENSP00000261769.4:n.*95T>C
ENST00000261769.9:c.*95T>C ENSP00000261769.4:n.*95T>C
ENST00000566612.5:c.*984T>C ENSP00000454782.1:n.*984T>C
ENST00000611625.4:c.*95T>C ENSP00000481063.1:n.*95T>C
ENST00000612417.4:c.1854-597T>C ENSP00000478360.1:n.1854-597T>C
ENST00000621016.4:c.1866-609T>C ENSP00000480664.1:n.1866-609T>C
NM_004360.3:c.*95T>C , LRG_301t1:c.*95T>C NP_004351.1:n.*95T>C
XM_011523488.1:c.*95T>C XP_011521790.1:n.*95T>C
XM_011523489.1:c.*95T>C XP_011521791.1:n.*95T>C
NM_001317184.1:c.*95T>C NP_001304113.1:n.*95T>C
NM_001317185.1:c.*95T>C NP_001304114.1:n.*95T>C
NM_001317186.1:c.*95T>C NP_001304115.1:n.*95T>C
NM_004360.4:c.*95T>C NP_004351.1:n.*95T>C
NM_004360.5:c.*95T>C MANE Select NP_004351.1:n.*95T>C
NM_001317184.2:c.*95T>C NP_001304113.1:n.*95T>C
NM_001317185.2:c.*95T>C NP_001304114.1:n.*95T>C
NM_001317186.2:c.*95T>C NP_001304115.1:n.*95T>C