Canonical Allele Identifier: CA2229980377
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68822044G= , CM000678.2:g.68822044G= GRCh38
NC_000016.9:g.68855947G= , CM000678.1:g.68855947G= GRCh37
NC_000016.8:g.67413448G= NCBI36
NG_008021.1:g.89753G= , LRG_301:g.89753G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1755G= MANE Select ENSP00000261769.4:p.Leu585=
ENST00000261769.9:c.1755G= ENSP00000261769.4:p.Leu585=
ENST00000422392.6:c.1572G= ENSP00000414946.2:p.Leu524=
ENST00000562836.5:n.1826G=
ENST00000566510.5:c.*421G= ENSP00000458139.1:n.*421G=
ENST00000566612.5:c.1609G= ENSP00000454782.1:p.Val537=
ENST00000611625.4:c.1818G= ENSP00000481063.1:p.Leu606=
ENST00000612417.4:c.1755G= ENSP00000478360.1:p.Leu585=
ENST00000621016.4:c.1755G= ENSP00000480664.1:p.Leu585=
NM_004360.3:c.1755G= , LRG_301t1:c.1755G= NP_004351.1:p.Leu585=
XM_011523488.1:c.1020G= XP_011521790.1:p.Leu340=
XM_011523489.1:c.1020G= XP_011521791.1:p.Leu340=
NM_001317184.1:c.1572G= NP_001304113.1:p.Leu524=
NM_001317185.1:c.207G= NP_001304114.1:p.Leu69=
NM_001317186.1:c.-211G= NP_001304115.1:n.-211G=
NM_004360.4:c.1755G= NP_004351.1:p.Leu585=
NM_004360.5:c.1755G= MANE Select NP_004351.1:p.Leu585=
NM_001317184.2:c.1572G= NP_001304113.1:p.Leu524=
NM_001317185.2:c.207G= NP_001304114.1:p.Leu69=
NM_001317186.2:c.-211G= NP_001304115.1:n.-211G=