Canonical Allele Identifier: CA396458678
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152131110
MyVariant Identifiers: chr16:g.68844187A>T (hg19) chr16:g.68810284A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810284A>T , CM000678.2:g.68810284A>T GRCh38
NC_000016.9:g.68844187A>T , CM000678.1:g.68844187A>T GRCh37
NC_000016.8:g.67401688A>T NCBI36
NG_008021.1:g.77993A>T , LRG_301:g.77993A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.775A>T MANE Select ENSP00000261769.4:p.Lys259Ter
ENST00000261769.9:c.775A>T ENSP00000261769.4:p.Lys259Ter
ENST00000422392.6:c.775A>T ENSP00000414946.2:p.Lys259Ter
ENST00000561751.1:c.455-1400A>T
ENST00000562836.5:n.846A>T
ENST00000566510.5:c.619A>T ENSP00000458139.1:p.Lys207Ter
ENST00000566612.5:c.775A>T ENSP00000454782.1:p.Lys259Ter
ENST00000611625.4:c.775A>T ENSP00000481063.1:p.Lys259Ter
ENST00000612417.4:c.775A>T ENSP00000478360.1:p.Lys259Ter
ENST00000621016.4:c.775A>T ENSP00000480664.1:p.Lys259Ter
NM_004360.3:c.775A>T , LRG_301t1:c.775A>T NP_004351.1:p.Lys259Ter
XM_011523488.1:c.40A>T XP_011521790.1:p.Lys14Ter
XM_011523489.1:c.40A>T XP_011521791.1:p.Lys14Ter
NM_001317184.1:c.775A>T NP_001304113.1:p.Lys259Ter
NM_001317185.1:c.-841A>T NP_001304114.1:n.-841A>T
NM_001317186.1:c.-1045A>T NP_001304115.1:n.-1045A>T
NM_004360.4:c.775A>T NP_004351.1:p.Lys259Ter
NM_004360.5:c.775A>T MANE Select NP_004351.1:p.Lys259Ter
NM_001317184.2:c.775A>T NP_001304113.1:p.Lys259Ter
NM_001317185.2:c.-841A>T NP_001304114.1:n.-841A>T
NM_001317186.2:c.-1045A>T NP_001304115.1:n.-1045A>T
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