Canonical Allele Identifier: CA396457339
Gene: CDH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.68835708T>G (hg19) chr16:g.68801805T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801805T>G , CM000678.2:g.68801805T>G GRCh38
NC_000016.9:g.68835708T>G , CM000678.1:g.68835708T>G GRCh37
NC_000016.8:g.67393209T>G NCBI36
NG_008021.1:g.69514T>G , LRG_301:g.69514T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.299T>G MANE Select ENSP00000261769.4:p.Val100Gly
ENST00000261769.9:c.299T>G ENSP00000261769.4:p.Val100Gly
ENST00000422392.6:c.299T>G ENSP00000414946.2:p.Val100Gly
ENST00000561751.1:c.66T>G
ENST00000562836.5:n.370T>G
ENST00000564676.5:n.581T>G
ENST00000564745.1:n.294T>G
ENST00000566510.5:c.299T>G ENSP00000458139.1:p.Val100Gly
ENST00000566612.5:c.299T>G ENSP00000454782.1:p.Val100Gly
ENST00000611625.4:c.299T>G ENSP00000481063.1:p.Val100Gly
ENST00000612417.4:c.299T>G ENSP00000478360.1:p.Val100Gly
ENST00000621016.4:c.299T>G ENSP00000480664.1:p.Val100Gly
NM_004360.3:c.299T>G , LRG_301t1:c.299T>G NP_004351.1:p.Val100Gly
XM_011523488.1:c.-437T>G XP_011521790.1:n.-437T>G
XM_011523489.1:c.-437T>G XP_011521791.1:n.-437T>G
NM_001317184.1:c.299T>G NP_001304113.1:p.Val100Gly
NM_001317185.1:c.-1317T>G NP_001304114.1:n.-1317T>G
NM_001317186.1:c.-1521T>G NP_001304115.1:n.-1521T>G
NM_004360.4:c.299T>G NP_004351.1:p.Val100Gly
NM_004360.5:c.299T>G MANE Select NP_004351.1:p.Val100Gly
NM_001317184.2:c.299T>G NP_001304113.1:p.Val100Gly
NM_001317185.2:c.-1317T>G NP_001304114.1:n.-1317T>G
NM_001317186.2:c.-1521T>G NP_001304115.1:n.-1521T>G
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