Canonical Allele Identifier: CA396472575
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152144135
MyVariant Identifiers: chr16:g.68867338T>A (hg19) chr16:g.68833435T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833435T>A , CM000678.2:g.68833435T>A GRCh38
NC_000016.9:g.68867338T>A , CM000678.1:g.68867338T>A GRCh37
NC_000016.8:g.67424839T>A NCBI36
NG_008021.1:g.101144T>A , LRG_301:g.101144T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2585T>A MANE Select ENSP00000261769.4:p.Leu862Ter
ENST00000261769.9:c.2585T>A ENSP00000261769.4:p.Leu862Ter
ENST00000422392.6:c.2402T>A ENSP00000414946.2:p.Leu801Ter
ENST00000562118.1:n.803T>A
ENST00000562836.5:n.2656T>A
ENST00000566510.5:c.*1251T>A ENSP00000458139.1:n.*1251T>A
ENST00000566612.5:c.*825T>A ENSP00000454782.1:n.*825T>A
ENST00000611625.4:c.2648T>A ENSP00000481063.1:p.Leu883Ter
ENST00000612417.4:c.1854-756T>A ENSP00000478360.1:n.1854-756T>A
ENST00000621016.4:c.1866-768T>A ENSP00000480664.1:n.1866-768T>A
NM_004360.3:c.2585T>A , LRG_301t1:c.2585T>A NP_004351.1:p.Leu862Ter
XM_011523488.1:c.1850T>A XP_011521790.1:p.Leu617Ter
XM_011523489.1:c.1850T>A XP_011521791.1:p.Leu617Ter
NM_001317184.1:c.2402T>A NP_001304113.1:p.Leu801Ter
NM_001317185.1:c.1037T>A NP_001304114.1:p.Leu346Ter
NM_001317186.1:c.620T>A NP_001304115.1:p.Leu207Ter
NM_004360.4:c.2585T>A NP_004351.1:p.Leu862Ter
NM_004360.5:c.2585T>A MANE Select NP_004351.1:p.Leu862Ter
NM_001317184.2:c.2402T>A NP_001304113.1:p.Leu801Ter
NM_001317185.2:c.1037T>A NP_001304114.1:p.Leu346Ter
NM_001317186.2:c.620T>A NP_001304115.1:p.Leu207Ter
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