Canonical Allele Identifier: CA396465023
Gene: CDH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.68853221T>C (hg19) chr16:g.68819318T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819318T>C , CM000678.2:g.68819318T>C GRCh38
NC_000016.9:g.68853221T>C , CM000678.1:g.68853221T>C GRCh37
NC_000016.8:g.67410722T>C NCBI36
NG_008021.1:g.87027T>C , LRG_301:g.87027T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1604T>C MANE Select ENSP00000261769.4:p.Ile535Thr
ENST00000261769.9:c.1604T>C ENSP00000261769.4:p.Ile535Thr
ENST00000422392.6:c.1421T>C ENSP00000414946.2:p.Ile474Thr
ENST00000562836.5:n.1675T>C
ENST00000566510.5:c.*270T>C ENSP00000458139.1:n.*270T>C
ENST00000566612.5:c.1566-2683T>C ENSP00000454782.1:n.1566-2683T>C
ENST00000611625.4:c.1667T>C ENSP00000481063.1:p.Ile556Thr
ENST00000612417.4:c.1604T>C ENSP00000478360.1:p.Ile535Thr
ENST00000621016.4:c.1604T>C ENSP00000480664.1:p.Ile535Thr
NM_004360.3:c.1604T>C , LRG_301t1:c.1604T>C NP_004351.1:p.Ile535Thr
XM_011523488.1:c.869T>C XP_011521790.1:p.Ile290Thr
XM_011523489.1:c.869T>C XP_011521791.1:p.Ile290Thr
NM_001317184.1:c.1421T>C NP_001304113.1:p.Ile474Thr
NM_001317185.1:c.56T>C NP_001304114.1:p.Ile19Thr
NM_001317186.1:c.-254-2683T>C NP_001304115.1:n.-254-2683T>C
NM_004360.4:c.1604T>C NP_004351.1:p.Ile535Thr
NM_004360.5:c.1604T>C MANE Select NP_004351.1:p.Ile535Thr
NM_001317184.2:c.1421T>C NP_001304113.1:p.Ile474Thr
NM_001317185.2:c.56T>C NP_001304114.1:p.Ile19Thr
NM_001317186.2:c.-254-2683T>C NP_001304115.1:n.-254-2683T>C
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