Canonical Allele Identifier: CA283319596
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs948215049

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833150C>A , CM000678.2:g.68833150C>A GRCh38
NC_000016.9:g.68867053C>A , CM000678.1:g.68867053C>A GRCh37
NC_000016.8:g.67424554C>A NCBI36
NG_008021.1:g.100859C>A , LRG_301:g.100859C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2440-140C>A MANE Select ENSP00000261769.4:n.2440-140C>A
ENST00000261769.9:c.2440-140C>A ENSP00000261769.4:n.2440-140C>A
ENST00000422392.6:c.2257-140C>A ENSP00000414946.2:n.2257-140C>A
ENST00000562118.1:n.658-140C>A
ENST00000562836.5:n.2511-140C>A
ENST00000566510.5:c.*1106-140C>A ENSP00000458139.1:n.*1106-140C>A
ENST00000566612.5:c.*680-140C>A ENSP00000454782.1:n.*680-140C>A
ENST00000611625.4:c.2503-140C>A ENSP00000481063.1:n.2503-140C>A
ENST00000612417.4:c.1854-1041C>A ENSP00000478360.1:n.1854-1041C>A
ENST00000621016.4:c.1866-1053C>A ENSP00000480664.1:n.1866-1053C>A
NM_004360.3:c.2440-140C>A , LRG_301t1:c.2440-140C>A NP_004351.1:n.2440-140C>A
XM_011523488.1:c.1705-140C>A XP_011521790.1:n.1705-140C>A
XM_011523489.1:c.1705-140C>A XP_011521791.1:n.1705-140C>A
NM_001317184.1:c.2257-140C>A NP_001304113.1:n.2257-140C>A
NM_001317185.1:c.892-140C>A NP_001304114.1:n.892-140C>A
NM_001317186.1:c.475-140C>A NP_001304115.1:n.475-140C>A
NM_004360.4:c.2440-140C>A NP_004351.1:n.2440-140C>A
NM_004360.5:c.2440-140C>A MANE Select NP_004351.1:n.2440-140C>A
NM_001317184.2:c.2257-140C>A NP_001304113.1:n.2257-140C>A
NM_001317185.2:c.892-140C>A NP_001304114.1:n.892-140C>A
NM_001317186.2:c.475-140C>A NP_001304115.1:n.475-140C>A