Canonical Allele Identifier: CA396472072
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152143895
MyVariant Identifiers: chr16:g.68867230C>A (hg19) chr16:g.68833327C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833327C>A , CM000678.2:g.68833327C>A GRCh38
NC_000016.9:g.68867230C>A , CM000678.1:g.68867230C>A GRCh37
NC_000016.8:g.67424731C>A NCBI36
NG_008021.1:g.101036C>A , LRG_301:g.101036C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2477C>A MANE Select ENSP00000261769.4:p.Pro826His
ENST00000261769.9:c.2477C>A ENSP00000261769.4:p.Pro826His
ENST00000422392.6:c.2294C>A ENSP00000414946.2:p.Pro765His
ENST00000562118.1:n.695C>A
ENST00000562836.5:n.2548C>A
ENST00000566510.5:c.*1143C>A ENSP00000458139.1:n.*1143C>A
ENST00000566612.5:c.*717C>A ENSP00000454782.1:n.*717C>A
ENST00000611625.4:c.2540C>A ENSP00000481063.1:p.Pro847His
ENST00000612417.4:c.1854-864C>A ENSP00000478360.1:n.1854-864C>A
ENST00000621016.4:c.1866-876C>A ENSP00000480664.1:n.1866-876C>A
NM_004360.3:c.2477C>A , LRG_301t1:c.2477C>A NP_004351.1:p.Pro826His
XM_011523488.1:c.1742C>A XP_011521790.1:p.Pro581His
XM_011523489.1:c.1742C>A XP_011521791.1:p.Pro581His
NM_001317184.1:c.2294C>A NP_001304113.1:p.Pro765His
NM_001317185.1:c.929C>A NP_001304114.1:p.Pro310His
NM_001317186.1:c.512C>A NP_001304115.1:p.Pro171His
NM_004360.4:c.2477C>A NP_004351.1:p.Pro826His
NM_004360.5:c.2477C>A MANE Select NP_004351.1:p.Pro826His
NM_001317184.2:c.2294C>A NP_001304113.1:p.Pro765His
NM_001317185.2:c.929C>A NP_001304114.1:p.Pro310His
NM_001317186.2:c.512C>A NP_001304115.1:p.Pro171His
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