Canonical Allele Identifier: CA2229980789
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68822159T= , CM000678.2:g.68822159T= GRCh38
NC_000016.9:g.68856062T= , CM000678.1:g.68856062T= GRCh37
NC_000016.8:g.67413563T= NCBI36
NG_008021.1:g.89868T= , LRG_301:g.89868T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1870T= MANE Select ENSP00000261769.4:p.Ser624=
ENST00000261769.9:c.1870T= ENSP00000261769.4:p.Ser624=
ENST00000422392.6:c.1687T= ENSP00000414946.2:p.Ser563=
ENST00000562836.5:n.1941T=
ENST00000566510.5:c.*536T= ENSP00000458139.1:n.*536T=
ENST00000566612.5:c.*110T= ENSP00000454782.1:n.*110T=
ENST00000611625.4:c.1933T= ENSP00000481063.1:p.Ser645=
ENST00000612417.4:c.1830+40T= ENSP00000478360.1:n.1830+40T=
ENST00000621016.4:c.1865+5T= ENSP00000480664.1:n.1865+5T=
NM_004360.3:c.1870T= , LRG_301t1:c.1870T= NP_004351.1:p.Ser624=
XM_011523488.1:c.1135T= XP_011521790.1:p.Ser379=
XM_011523489.1:c.1135T= XP_011521791.1:p.Ser379=
NM_001317184.1:c.1687T= NP_001304113.1:p.Ser563=
NM_001317185.1:c.322T= NP_001304114.1:p.Ser108=
NM_001317186.1:c.-96T= NP_001304115.1:n.-96T=
NM_004360.4:c.1870T= NP_004351.1:p.Ser624=
NM_004360.5:c.1870T= MANE Select NP_004351.1:p.Ser624=
NM_001317184.2:c.1687T= NP_001304113.1:p.Ser563=
NM_001317185.2:c.322T= NP_001304114.1:p.Ser108=
NM_001317186.2:c.-96T= NP_001304115.1:n.-96T=