Canonical Allele Identifier: CA2229980587
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68822097G= , CM000678.2:g.68822097G= GRCh38
NC_000016.9:g.68856000G= , CM000678.1:g.68856000G= GRCh37
NC_000016.8:g.67413501G= NCBI36
NG_008021.1:g.89806G= , LRG_301:g.89806G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1808G= MANE Select ENSP00000261769.4:p.Cys603=
ENST00000261769.9:c.1808G= ENSP00000261769.4:p.Cys603=
ENST00000422392.6:c.1625G= ENSP00000414946.2:p.Cys542=
ENST00000562836.5:n.1879G=
ENST00000566510.5:c.*474G= ENSP00000458139.1:n.*474G=
ENST00000566612.5:c.*48G= ENSP00000454782.1:n.*48G=
ENST00000611625.4:c.1871G= ENSP00000481063.1:p.Cys624=
ENST00000612417.4:c.1808G= ENSP00000478360.1:p.Cys603=
ENST00000621016.4:c.1808G= ENSP00000480664.1:p.Cys603=
NM_004360.3:c.1808G= , LRG_301t1:c.1808G= NP_004351.1:p.Cys603=
XM_011523488.1:c.1073G= XP_011521790.1:p.Cys358=
XM_011523489.1:c.1073G= XP_011521791.1:p.Cys358=
NM_001317184.1:c.1625G= NP_001304113.1:p.Cys542=
NM_001317185.1:c.260G= NP_001304114.1:p.Cys87=
NM_001317186.1:c.-158G= NP_001304115.1:n.-158G=
NM_004360.4:c.1808G= NP_004351.1:p.Cys603=
NM_004360.5:c.1808G= MANE Select NP_004351.1:p.Cys603=
NM_001317184.2:c.1625G= NP_001304113.1:p.Cys542=
NM_001317185.2:c.260G= NP_001304114.1:p.Cys87=
NM_001317186.2:c.-158G= NP_001304115.1:n.-158G=