Canonical Allele Identifier: CA396465244
Gene: CDH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.68853274T>G (hg19) chr16:g.68819371T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819371T>G , CM000678.2:g.68819371T>G GRCh38
NC_000016.9:g.68853274T>G , CM000678.1:g.68853274T>G GRCh37
NC_000016.8:g.67410775T>G NCBI36
NG_008021.1:g.87080T>G , LRG_301:g.87080T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1657T>G MANE Select ENSP00000261769.4:p.Phe553Val
ENST00000261769.9:c.1657T>G ENSP00000261769.4:p.Phe553Val
ENST00000422392.6:c.1474T>G ENSP00000414946.2:p.Phe492Val
ENST00000562836.5:n.1728T>G
ENST00000566510.5:c.*323T>G ENSP00000458139.1:n.*323T>G
ENST00000566612.5:c.1566-2630T>G ENSP00000454782.1:n.1566-2630T>G
ENST00000611625.4:c.1720T>G ENSP00000481063.1:p.Phe574Val
ENST00000612417.4:c.1657T>G ENSP00000478360.1:p.Phe553Val
ENST00000621016.4:c.1657T>G ENSP00000480664.1:p.Phe553Val
NM_004360.3:c.1657T>G , LRG_301t1:c.1657T>G NP_004351.1:p.Phe553Val
XM_011523488.1:c.922T>G XP_011521790.1:p.Phe308Val
XM_011523489.1:c.922T>G XP_011521791.1:p.Phe308Val
NM_001317184.1:c.1474T>G NP_001304113.1:p.Phe492Val
NM_001317185.1:c.109T>G NP_001304114.1:p.Phe37Val
NM_001317186.1:c.-254-2630T>G NP_001304115.1:n.-254-2630T>G
NM_004360.4:c.1657T>G NP_004351.1:p.Phe553Val
NM_004360.5:c.1657T>G MANE Select NP_004351.1:p.Phe553Val
NM_001317184.2:c.1474T>G NP_001304113.1:p.Phe492Val
NM_001317185.2:c.109T>G NP_001304114.1:p.Phe37Val
NM_001317186.2:c.-254-2630T>G NP_001304115.1:n.-254-2630T>G
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