Canonical Allele Identifier: CA396471290
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152142446
MyVariant Identifiers: chr16:g.68863678A>T (hg19) chr16:g.68829775A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829775A>T , CM000678.2:g.68829775A>T GRCh38
NC_000016.9:g.68863678A>T , CM000678.1:g.68863678A>T GRCh37
NC_000016.8:g.67421179A>T NCBI36
NG_008021.1:g.97484A>T , LRG_301:g.97484A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2417A>T MANE Select ENSP00000261769.4:p.Glu806Val
ENST00000261769.9:c.2417A>T ENSP00000261769.4:p.Glu806Val
ENST00000422392.6:c.2234A>T ENSP00000414946.2:p.Glu745Val
ENST00000562118.1:n.635A>T
ENST00000562836.5:n.2488A>T
ENST00000566510.5:c.*1083A>T ENSP00000458139.1:n.*1083A>T
ENST00000566612.5:c.*657A>T ENSP00000454782.1:n.*657A>T
ENST00000611625.4:c.2480A>T ENSP00000481063.1:p.Glu827Val
ENST00000612417.4:c.1853+3221A>T ENSP00000478360.1:n.1853+3221A>T
ENST00000621016.4:c.1866-4428A>T ENSP00000480664.1:n.1866-4428A>T
NM_004360.3:c.2417A>T , LRG_301t1:c.2417A>T NP_004351.1:p.Glu806Val
XM_011523488.1:c.1682A>T XP_011521790.1:p.Glu561Val
XM_011523489.1:c.1682A>T XP_011521791.1:p.Glu561Val
NM_001317184.1:c.2234A>T NP_001304113.1:p.Glu745Val
NM_001317185.1:c.869A>T NP_001304114.1:p.Glu290Val
NM_001317186.1:c.452A>T NP_001304115.1:p.Glu151Val
NM_004360.4:c.2417A>T NP_004351.1:p.Glu806Val
NM_004360.5:c.2417A>T MANE Select NP_004351.1:p.Glu806Val
NM_001317184.2:c.2234A>T NP_001304113.1:p.Glu745Val
NM_001317185.2:c.869A>T NP_001304114.1:p.Glu290Val
NM_001317186.2:c.452A>T NP_001304115.1:p.Glu151Val
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