Canonical Allele Identifier: CA396472034
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs878854686
gnomAD v4: 16-68833317-A-T
MyVariant Identifiers: chr16:g.68867220A>T (hg19) chr16:g.68833317A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833317A>T , CM000678.2:g.68833317A>T GRCh38
NC_000016.9:g.68867220A>T , CM000678.1:g.68867220A>T GRCh37
NC_000016.8:g.67424721A>T NCBI36
NG_008021.1:g.101026A>T , LRG_301:g.101026A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2467A>T MANE Select ENSP00000261769.4:p.Thr823Ser
ENST00000261769.9:c.2467A>T ENSP00000261769.4:p.Thr823Ser
ENST00000422392.6:c.2284A>T ENSP00000414946.2:p.Thr762Ser
ENST00000562118.1:n.685A>T
ENST00000562836.5:n.2538A>T
ENST00000566510.5:c.*1133A>T ENSP00000458139.1:n.*1133A>T
ENST00000566612.5:c.*707A>T ENSP00000454782.1:n.*707A>T
ENST00000611625.4:c.2530A>T ENSP00000481063.1:p.Thr844Ser
ENST00000612417.4:c.1854-874A>T ENSP00000478360.1:n.1854-874A>T
ENST00000621016.4:c.1866-886A>T ENSP00000480664.1:n.1866-886A>T
NM_004360.3:c.2467A>T , LRG_301t1:c.2467A>T NP_004351.1:p.Thr823Ser
XM_011523488.1:c.1732A>T XP_011521790.1:p.Thr578Ser
XM_011523489.1:c.1732A>T XP_011521791.1:p.Thr578Ser
NM_001317184.1:c.2284A>T NP_001304113.1:p.Thr762Ser
NM_001317185.1:c.919A>T NP_001304114.1:p.Thr307Ser
NM_001317186.1:c.502A>T NP_001304115.1:p.Thr168Ser
NM_004360.4:c.2467A>T NP_004351.1:p.Thr823Ser
NM_004360.5:c.2467A>T MANE Select NP_004351.1:p.Thr823Ser
NM_001317184.2:c.2284A>T NP_001304113.1:p.Thr762Ser
NM_001317185.2:c.919A>T NP_001304114.1:p.Thr307Ser
NM_001317186.2:c.502A>T NP_001304115.1:p.Thr168Ser
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