Canonical Allele Identifier: CA2732912546
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152144355

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833558C>T , CM000678.2:g.68833558C>T GRCh38
NC_000016.9:g.68867461C>T , CM000678.1:g.68867461C>T GRCh37
NC_000016.8:g.67424962C>T NCBI36
NG_008021.1:g.101267C>T , LRG_301:g.101267C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.*59C>T MANE Select ENSP00000261769.4:n.*59C>T
ENST00000261769.9:c.*59C>T ENSP00000261769.4:n.*59C>T
ENST00000562118.1:n.926C>T
ENST00000566612.5:c.*948C>T ENSP00000454782.1:n.*948C>T
ENST00000611625.4:c.*59C>T ENSP00000481063.1:n.*59C>T
ENST00000612417.4:c.1854-633C>T ENSP00000478360.1:n.1854-633C>T
ENST00000621016.4:c.1866-645C>T ENSP00000480664.1:n.1866-645C>T
NM_004360.3:c.*59C>T , LRG_301t1:c.*59C>T NP_004351.1:n.*59C>T
XM_011523488.1:c.*59C>T XP_011521790.1:n.*59C>T
XM_011523489.1:c.*59C>T XP_011521791.1:n.*59C>T
NM_001317184.1:c.*59C>T NP_001304113.1:n.*59C>T
NM_001317185.1:c.*59C>T NP_001304114.1:n.*59C>T
NM_001317186.1:c.*59C>T NP_001304115.1:n.*59C>T
NM_004360.4:c.*59C>T NP_004351.1:n.*59C>T
NM_004360.5:c.*59C>T MANE Select NP_004351.1:n.*59C>T
NM_001317184.2:c.*59C>T NP_001304113.1:n.*59C>T
NM_001317185.2:c.*59C>T NP_001304114.1:n.*59C>T
NM_001317186.2:c.*59C>T NP_001304115.1:n.*59C>T