Canonical Allele Identifier: CA2229978414
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833431T= , CM000678.2:g.68833431T= GRCh38
NC_000016.9:g.68867334T= , CM000678.1:g.68867334T= GRCh37
NC_000016.8:g.67424835T= NCBI36
NG_008021.1:g.101140T= , LRG_301:g.101140T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2581T= MANE Select ENSP00000261769.4:p.Tyr861=
ENST00000261769.9:c.2581T= ENSP00000261769.4:p.Tyr861=
ENST00000422392.6:c.2398T= ENSP00000414946.2:p.Tyr800=
ENST00000562118.1:n.799T=
ENST00000562836.5:n.2652T=
ENST00000566510.5:c.*1247T= ENSP00000458139.1:n.*1247T=
ENST00000566612.5:c.*821T= ENSP00000454782.1:n.*821T=
ENST00000611625.4:c.2644T= ENSP00000481063.1:p.Tyr882=
ENST00000612417.4:c.1854-760T= ENSP00000478360.1:n.1854-760T=
ENST00000621016.4:c.1866-772T= ENSP00000480664.1:n.1866-772T=
NM_004360.3:c.2581T= , LRG_301t1:c.2581T= NP_004351.1:p.Tyr861=
XM_011523488.1:c.1846T= XP_011521790.1:p.Tyr616=
XM_011523489.1:c.1846T= XP_011521791.1:p.Tyr616=
NM_001317184.1:c.2398T= NP_001304113.1:p.Tyr800=
NM_001317185.1:c.1033T= NP_001304114.1:p.Tyr345=
NM_001317186.1:c.616T= NP_001304115.1:p.Tyr206=
NM_004360.4:c.2581T= NP_004351.1:p.Tyr861=
NM_004360.5:c.2581T= MANE Select NP_004351.1:p.Tyr861=
NM_001317184.2:c.2398T= NP_001304113.1:p.Tyr800=
NM_001317185.2:c.1033T= NP_001304114.1:p.Tyr345=
NM_001317186.2:c.616T= NP_001304115.1:p.Tyr206=