Canonical Allele Identifier: CA396457374
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152126917
MyVariant Identifiers: chr16:g.68835726C>G (hg19) chr16:g.68801823C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801823C>G , CM000678.2:g.68801823C>G GRCh38
NC_000016.9:g.68835726C>G , CM000678.1:g.68835726C>G GRCh37
NC_000016.8:g.67393227C>G NCBI36
NG_008021.1:g.69532C>G , LRG_301:g.69532C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.317C>G MANE Select ENSP00000261769.4:p.Thr106Ser
ENST00000261769.9:c.317C>G ENSP00000261769.4:p.Thr106Ser
ENST00000422392.6:c.317C>G ENSP00000414946.2:p.Thr106Ser
ENST00000561751.1:c.84C>G
ENST00000562836.5:n.388C>G
ENST00000564676.5:n.599C>G
ENST00000564745.1:n.312C>G
ENST00000566510.5:c.317C>G ENSP00000458139.1:p.Thr106Ser
ENST00000566612.5:c.317C>G ENSP00000454782.1:p.Thr106Ser
ENST00000611625.4:c.317C>G ENSP00000481063.1:p.Thr106Ser
ENST00000612417.4:c.317C>G ENSP00000478360.1:p.Thr106Ser
ENST00000621016.4:c.317C>G ENSP00000480664.1:p.Thr106Ser
NM_004360.3:c.317C>G , LRG_301t1:c.317C>G NP_004351.1:p.Thr106Ser
XM_011523488.1:c.-419C>G XP_011521790.1:n.-419C>G
XM_011523489.1:c.-419C>G XP_011521791.1:n.-419C>G
NM_001317184.1:c.317C>G NP_001304113.1:p.Thr106Ser
NM_001317185.1:c.-1299C>G NP_001304114.1:n.-1299C>G
NM_001317186.1:c.-1503C>G NP_001304115.1:n.-1503C>G
NM_004360.4:c.317C>G NP_004351.1:p.Thr106Ser
NM_004360.5:c.317C>G MANE Select NP_004351.1:p.Thr106Ser
NM_001317184.2:c.317C>G NP_001304113.1:p.Thr106Ser
NM_001317185.2:c.-1299C>G NP_001304114.1:n.-1299C>G
NM_001317186.2:c.-1503C>G NP_001304115.1:n.-1503C>G
Search 100 bp 5'
Search 100 bp 3'