Canonical Allele Identifier: CA396467614
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1275496047

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68823452A>T , CM000678.2:g.68823452A>T GRCh38
NC_000016.9:g.68857355A>T , CM000678.1:g.68857355A>T GRCh37
NC_000016.8:g.67414856A>T NCBI36
NG_008021.1:g.91161A>T , LRG_301:g.91161A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1990A>T MANE Select ENSP00000261769.4:p.Lys664Ter
ENST00000261769.9:c.1990A>T ENSP00000261769.4:p.Lys664Ter
ENST00000422392.6:c.1807A>T ENSP00000414946.2:p.Lys603Ter
ENST00000562118.1:n.208A>T
ENST00000562836.5:n.2061A>T
ENST00000566510.5:c.*656A>T ENSP00000458139.1:n.*656A>T
ENST00000566612.5:c.*230A>T ENSP00000454782.1:n.*230A>T
ENST00000611625.4:c.2053A>T ENSP00000481063.1:p.Lys685Ter
ENST00000612417.4:c.1830+1333A>T ENSP00000478360.1:n.1830+1333A>T
ENST00000621016.4:c.1865+1298A>T ENSP00000480664.1:n.1865+1298A>T
NM_004360.3:c.1990A>T , LRG_301t1:c.1990A>T NP_004351.1:p.Lys664Ter
XM_011523488.1:c.1255A>T XP_011521790.1:p.Lys419Ter
XM_011523489.1:c.1255A>T XP_011521791.1:p.Lys419Ter
NM_001317184.1:c.1807A>T NP_001304113.1:p.Lys603Ter
NM_001317185.1:c.442A>T NP_001304114.1:p.Lys148Ter
NM_001317186.1:c.25A>T NP_001304115.1:p.Lys9Ter
NM_004360.4:c.1990A>T NP_004351.1:p.Lys664Ter
NM_004360.5:c.1990A>T MANE Select NP_004351.1:p.Lys664Ter
NM_001317184.2:c.1807A>T NP_001304113.1:p.Lys603Ter
NM_001317185.2:c.442A>T NP_001304114.1:p.Lys148Ter
NM_001317186.2:c.25A>T NP_001304115.1:p.Lys9Ter