Canonical Allele Identifier: CA396471998
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152143857
MyVariant Identifiers: chr16:g.68867210T>G (hg19) chr16:g.68833307T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833307T>G , CM000678.2:g.68833307T>G GRCh38
NC_000016.9:g.68867210T>G , CM000678.1:g.68867210T>G GRCh37
NC_000016.8:g.67424711T>G NCBI36
NG_008021.1:g.101016T>G , LRG_301:g.101016T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2457T>G MANE Select ENSP00000261769.4:p.Asp819Glu
ENST00000261769.9:c.2457T>G ENSP00000261769.4:p.Asp819Glu
ENST00000422392.6:c.2274T>G ENSP00000414946.2:p.Asp758Glu
ENST00000562118.1:n.675T>G
ENST00000562836.5:n.2528T>G
ENST00000566510.5:c.*1123T>G ENSP00000458139.1:n.*1123T>G
ENST00000566612.5:c.*697T>G ENSP00000454782.1:n.*697T>G
ENST00000611625.4:c.2520T>G ENSP00000481063.1:p.Asp840Glu
ENST00000612417.4:c.1854-884T>G ENSP00000478360.1:n.1854-884T>G
ENST00000621016.4:c.1866-896T>G ENSP00000480664.1:n.1866-896T>G
NM_004360.3:c.2457T>G , LRG_301t1:c.2457T>G NP_004351.1:p.Asp819Glu
XM_011523488.1:c.1722T>G XP_011521790.1:p.Asp574Glu
XM_011523489.1:c.1722T>G XP_011521791.1:p.Asp574Glu
NM_001317184.1:c.2274T>G NP_001304113.1:p.Asp758Glu
NM_001317185.1:c.909T>G NP_001304114.1:p.Asp303Glu
NM_001317186.1:c.492T>G NP_001304115.1:p.Asp164Glu
NM_004360.4:c.2457T>G NP_004351.1:p.Asp819Glu
NM_004360.5:c.2457T>G MANE Select NP_004351.1:p.Asp819Glu
NM_001317184.2:c.2274T>G NP_001304113.1:p.Asp758Glu
NM_001317185.2:c.909T>G NP_001304114.1:p.Asp303Glu
NM_001317186.2:c.492T>G NP_001304115.1:p.Asp164Glu
Search 100 bp 5'
Search 100 bp 3'