Canonical Allele Identifier: CA2229977920
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1596975779
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68832965G>C , CM000678.2:g.68832965G>C GRCh38
NC_000016.9:g.68866868G>C , CM000678.1:g.68866868G>C GRCh37
NC_000016.8:g.67424369G>C NCBI36
NG_008021.1:g.100674G>C , LRG_301:g.100674G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2440-325G>C MANE Select ENSP00000261769.4:n.2440-325G>C
ENST00000261769.9:c.2440-325G>C ENSP00000261769.4:n.2440-325G>C
ENST00000422392.6:c.2257-325G>C ENSP00000414946.2:n.2257-325G>C
ENST00000562118.1:n.658-325G>C
ENST00000562836.5:n.2511-325G>C
ENST00000566510.5:c.*1106-325G>C ENSP00000458139.1:n.*1106-325G>C
ENST00000566612.5:c.*680-325G>C ENSP00000454782.1:n.*680-325G>C
ENST00000611625.4:c.2503-325G>C ENSP00000481063.1:n.2503-325G>C
ENST00000612417.4:c.1854-1226G>C ENSP00000478360.1:n.1854-1226G>C
ENST00000621016.4:c.1866-1238G>C ENSP00000480664.1:n.1866-1238G>C
NM_004360.3:c.2440-325G>C , LRG_301t1:c.2440-325G>C NP_004351.1:n.2440-325G>C
XM_011523488.1:c.1705-325G>C XP_011521790.1:n.1705-325G>C
XM_011523489.1:c.1705-325G>C XP_011521791.1:n.1705-325G>C
NM_001317184.1:c.2257-325G>C NP_001304113.1:n.2257-325G>C
NM_001317185.1:c.892-325G>C NP_001304114.1:n.892-325G>C
NM_001317186.1:c.475-325G>C NP_001304115.1:n.475-325G>C
NM_004360.4:c.2440-325G>C NP_004351.1:n.2440-325G>C
NM_004360.5:c.2440-325G>C MANE Select NP_004351.1:n.2440-325G>C
NM_001317184.2:c.2257-325G>C NP_001304113.1:n.2257-325G>C
NM_001317185.2:c.892-325G>C NP_001304114.1:n.892-325G>C
NM_001317186.2:c.475-325G>C NP_001304115.1:n.475-325G>C
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