Canonical Allele Identifier: CA396461389
Gene: CDH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.68847303T>A (hg19) chr16:g.68813400T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68813400T>A , CM000678.2:g.68813400T>A GRCh38
NC_000016.9:g.68847303T>A , CM000678.1:g.68847303T>A GRCh37
NC_000016.8:g.67404804T>A NCBI36
NG_008021.1:g.81109T>A , LRG_301:g.81109T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1225T>A MANE Select ENSP00000261769.4:p.Trp409Arg
ENST00000261769.9:c.1225T>A ENSP00000261769.4:p.Trp409Arg
ENST00000422392.6:c.1137+1137T>A ENSP00000414946.2:n.1137+1137T>A
ENST00000562836.5:n.1296T>A
ENST00000565810.1:n.269T>A
ENST00000566510.5:c.1069T>A ENSP00000458139.1:p.Trp357Arg
ENST00000566612.5:c.1225T>A ENSP00000454782.1:p.Trp409Arg
ENST00000611625.4:c.1225T>A ENSP00000481063.1:p.Trp409Arg
ENST00000612417.4:c.1225T>A ENSP00000478360.1:p.Trp409Arg
ENST00000621016.4:c.1225T>A ENSP00000480664.1:p.Trp409Arg
NM_004360.3:c.1225T>A , LRG_301t1:c.1225T>A NP_004351.1:p.Trp409Arg
XM_011523488.1:c.490T>A XP_011521790.1:p.Trp164Arg
XM_011523489.1:c.490T>A XP_011521791.1:p.Trp164Arg
NM_001317184.1:c.1137+1137T>A NP_001304113.1:n.1137+1137T>A
NM_001317185.1:c.-391T>A NP_001304114.1:n.-391T>A
NM_001317186.1:c.-595T>A NP_001304115.1:n.-595T>A
NM_004360.4:c.1225T>A NP_004351.1:p.Trp409Arg
NM_004360.5:c.1225T>A MANE Select NP_004351.1:p.Trp409Arg
NM_001317184.2:c.1137+1137T>A NP_001304113.1:n.1137+1137T>A
NM_001317185.2:c.-391T>A NP_001304114.1:n.-391T>A
NM_001317186.2:c.-595T>A NP_001304115.1:n.-595T>A
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