Canonical Allele Identifier: CA396457870
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs201141645
MyVariant Identifiers: chr16:g.68842610A>T (hg19) chr16:g.68808707A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68808707A>T , CM000678.2:g.68808707A>T GRCh38
NC_000016.9:g.68842610A>T , CM000678.1:g.68842610A>T GRCh37
NC_000016.8:g.67400111A>T NCBI36
NG_008021.1:g.76416A>T , LRG_301:g.76416A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.546A>T MANE Select ENSP00000261769.4:p.Lys182Asn
ENST00000261769.9:c.546A>T ENSP00000261769.4:p.Lys182Asn
ENST00000422392.6:c.546A>T ENSP00000414946.2:p.Lys182Asn
ENST00000561751.1:c.313A>T
ENST00000562836.5:n.617A>T
ENST00000564676.5:n.828A>T
ENST00000564745.1:n.541A>T
ENST00000566510.5:c.531+140A>T ENSP00000458139.1:n.531+140A>T
ENST00000566612.5:c.546A>T ENSP00000454782.1:p.Lys182Asn
ENST00000567320.1:n.56A>T
ENST00000611625.4:c.546A>T ENSP00000481063.1:p.Lys182Asn
ENST00000612417.4:c.546A>T ENSP00000478360.1:p.Lys182Asn
ENST00000621016.4:c.546A>T ENSP00000480664.1:p.Lys182Asn
NM_004360.3:c.546A>T , LRG_301t1:c.546A>T NP_004351.1:p.Lys182Asn
XM_011523488.1:c.-190A>T XP_011521790.1:n.-190A>T
XM_011523489.1:c.-190A>T XP_011521791.1:n.-190A>T
NM_001317184.1:c.546A>T NP_001304113.1:p.Lys182Asn
NM_001317185.1:c.-1070A>T NP_001304114.1:n.-1070A>T
NM_001317186.1:c.-1274A>T NP_001304115.1:n.-1274A>T
NM_004360.4:c.546A>T NP_004351.1:p.Lys182Asn
NM_004360.5:c.546A>T MANE Select NP_004351.1:p.Lys182Asn
NM_001317184.2:c.546A>T NP_001304113.1:p.Lys182Asn
NM_001317185.2:c.-1070A>T NP_001304114.1:n.-1070A>T
NM_001317186.2:c.-1274A>T NP_001304115.1:n.-1274A>T
Search 100 bp 5'
Search 100 bp 3'