Canonical Allele Identifier: CA396472727
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152144186

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833460G>T , CM000678.2:g.68833460G>T GRCh38
NC_000016.9:g.68867363G>T , CM000678.1:g.68867363G>T GRCh37
NC_000016.8:g.67424864G>T NCBI36
NG_008021.1:g.101169G>T , LRG_301:g.101169G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2610G>T MANE Select ENSP00000261769.4:p.Lys870Asn
ENST00000261769.9:c.2610G>T ENSP00000261769.4:p.Lys870Asn
ENST00000422392.6:c.2427G>T ENSP00000414946.2:p.Lys809Asn
ENST00000562118.1:n.828G>T
ENST00000562836.5:n.2681G>T
ENST00000566510.5:c.*1276G>T ENSP00000458139.1:n.*1276G>T
ENST00000566612.5:c.*850G>T ENSP00000454782.1:n.*850G>T
ENST00000611625.4:c.2673G>T ENSP00000481063.1:p.Lys891Asn
ENST00000612417.4:c.1854-731G>T ENSP00000478360.1:n.1854-731G>T
ENST00000621016.4:c.1866-743G>T ENSP00000480664.1:n.1866-743G>T
NM_004360.3:c.2610G>T , LRG_301t1:c.2610G>T NP_004351.1:p.Lys870Asn
XM_011523488.1:c.1875G>T XP_011521790.1:p.Lys625Asn
XM_011523489.1:c.1875G>T XP_011521791.1:p.Lys625Asn
NM_001317184.1:c.2427G>T NP_001304113.1:p.Lys809Asn
NM_001317185.1:c.1062G>T NP_001304114.1:p.Lys354Asn
NM_001317186.1:c.645G>T NP_001304115.1:p.Lys215Asn
NM_004360.4:c.2610G>T NP_004351.1:p.Lys870Asn
NM_004360.5:c.2610G>T MANE Select NP_004351.1:p.Lys870Asn
NM_001317184.2:c.2427G>T NP_001304113.1:p.Lys809Asn
NM_001317185.2:c.1062G>T NP_001304114.1:p.Lys354Asn
NM_001317186.2:c.645G>T NP_001304115.1:p.Lys215Asn