Canonical Allele Identifier: CA14224291
Gene: CDH1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10431923

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68805360G>T , CM000678.2:g.68805360G>T GRCh38
NC_000016.9:g.68839263G>T , CM000678.1:g.68839263G>T GRCh37
NC_000016.8:g.67396764G>T NCBI36
NG_008021.1:g.73069G>T , LRG_301:g.73069G>T

Transcript Alleles

HGVS Amino-acid change
NM_004360.3:c.388-3064G>T , LRG_301t1:c.388-3064G>T
XM_011523488.1:c.-348-3064G>T XP_011521790.1:p.=
XM_011523489.1:c.-348-3064G>T XP_011521791.1:p.=
NM_001317184.1:c.388-3064G>T VV NP_001304113.1:p.=
NM_001317185.1:c.-1228-3064G>T VV NP_001304114.1:p.=
NM_001317186.1:c.-1432-3064G>T VV NP_001304115.1:p.=
NM_004360.4:c.388-3064G>T VV NP_004351.1:p.=
ENST00000261769.9:c.388-3064G>T ENSP00000261769.4:p.=
ENST00000422392.6:c.388-3064G>T ENSP00000414946.2:p.=
ENST00000561751.1:n.155-3064G>T
ENST00000562836.5:n.459-3064G>T
ENST00000564676.5:n.670-3064G>T
ENST00000564745.1:n.383-3064G>T
ENST00000566510.5:c.388-3064G>T ENSP00000458139.1:p.=
ENST00000566612.5:c.388-3064G>T ENSP00000454782.1:p.=
ENST00000611625.4:c.388-3064G>T ENSP00000481063.1:p.=
ENST00000612417.4:c.388-3064G>T ENSP00000478360.1:p.=
ENST00000621016.4:c.388-3064G>T ENSP00000480664.1:p.=