Canonical Allele Identifier: CA396472059
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs587781312
MyVariant Identifiers: chr16:g.68867227C>A (hg19) chr16:g.68833324C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833324C>A , CM000678.2:g.68833324C>A GRCh38
NC_000016.9:g.68867227C>A , CM000678.1:g.68867227C>A GRCh37
NC_000016.8:g.67424728C>A NCBI36
NG_008021.1:g.101033C>A , LRG_301:g.101033C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2474C>A MANE Select ENSP00000261769.4:p.Pro825Gln
ENST00000261769.9:c.2474C>A ENSP00000261769.4:p.Pro825Gln
ENST00000422392.6:c.2291C>A ENSP00000414946.2:p.Pro764Gln
ENST00000562118.1:n.692C>A
ENST00000562836.5:n.2545C>A
ENST00000566510.5:c.*1140C>A ENSP00000458139.1:n.*1140C>A
ENST00000566612.5:c.*714C>A ENSP00000454782.1:n.*714C>A
ENST00000611625.4:c.2537C>A ENSP00000481063.1:p.Pro846Gln
ENST00000612417.4:c.1854-867C>A ENSP00000478360.1:n.1854-867C>A
ENST00000621016.4:c.1866-879C>A ENSP00000480664.1:n.1866-879C>A
NM_004360.3:c.2474C>A , LRG_301t1:c.2474C>A NP_004351.1:p.Pro825Gln
XM_011523488.1:c.1739C>A XP_011521790.1:p.Pro580Gln
XM_011523489.1:c.1739C>A XP_011521791.1:p.Pro580Gln
NM_001317184.1:c.2291C>A NP_001304113.1:p.Pro764Gln
NM_001317185.1:c.926C>A NP_001304114.1:p.Pro309Gln
NM_001317186.1:c.509C>A NP_001304115.1:p.Pro170Gln
NM_004360.4:c.2474C>A NP_004351.1:p.Pro825Gln
NM_004360.5:c.2474C>A MANE Select NP_004351.1:p.Pro825Gln
NM_001317184.2:c.2291C>A NP_001304113.1:p.Pro764Gln
NM_001317185.2:c.926C>A NP_001304114.1:p.Pro309Gln
NM_001317186.2:c.509C>A NP_001304115.1:p.Pro170Gln
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