Canonical Allele Identifier: CA396457344
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152126877
MyVariant Identifiers: chr16:g.68835711A>T (hg19) chr16:g.68801808A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801808A>T , CM000678.2:g.68801808A>T GRCh38
NC_000016.9:g.68835711A>T , CM000678.1:g.68835711A>T GRCh37
NC_000016.8:g.67393212A>T NCBI36
NG_008021.1:g.69517A>T , LRG_301:g.69517A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.302A>T MANE Select ENSP00000261769.4:p.Tyr101Phe
ENST00000261769.9:c.302A>T ENSP00000261769.4:p.Tyr101Phe
ENST00000422392.6:c.302A>T ENSP00000414946.2:p.Tyr101Phe
ENST00000561751.1:c.69A>T
ENST00000562836.5:n.373A>T
ENST00000564676.5:n.584A>T
ENST00000564745.1:n.297A>T
ENST00000566510.5:c.302A>T ENSP00000458139.1:p.Tyr101Phe
ENST00000566612.5:c.302A>T ENSP00000454782.1:p.Tyr101Phe
ENST00000611625.4:c.302A>T ENSP00000481063.1:p.Tyr101Phe
ENST00000612417.4:c.302A>T ENSP00000478360.1:p.Tyr101Phe
ENST00000621016.4:c.302A>T ENSP00000480664.1:p.Tyr101Phe
NM_004360.3:c.302A>T , LRG_301t1:c.302A>T NP_004351.1:p.Tyr101Phe
XM_011523488.1:c.-434A>T XP_011521790.1:n.-434A>T
XM_011523489.1:c.-434A>T XP_011521791.1:n.-434A>T
NM_001317184.1:c.302A>T NP_001304113.1:p.Tyr101Phe
NM_001317185.1:c.-1314A>T NP_001304114.1:n.-1314A>T
NM_001317186.1:c.-1518A>T NP_001304115.1:n.-1518A>T
NM_004360.4:c.302A>T NP_004351.1:p.Tyr101Phe
NM_004360.5:c.302A>T MANE Select NP_004351.1:p.Tyr101Phe
NM_001317184.2:c.302A>T NP_001304113.1:p.Tyr101Phe
NM_001317185.2:c.-1314A>T NP_001304114.1:n.-1314A>T
NM_001317186.2:c.-1518A>T NP_001304115.1:n.-1518A>T
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