Canonical Allele Identifier: CA2229978171
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833353T= , CM000678.2:g.68833353T= GRCh38
NC_000016.9:g.68867256T= , CM000678.1:g.68867256T= GRCh37
NC_000016.8:g.67424757T= NCBI36
NG_008021.1:g.101062T= , LRG_301:g.101062T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2503T= MANE Select ENSP00000261769.4:p.Tyr835=
ENST00000261769.9:c.2503T= ENSP00000261769.4:p.Tyr835=
ENST00000422392.6:c.2320T= ENSP00000414946.2:p.Tyr774=
ENST00000562118.1:n.721T=
ENST00000562836.5:n.2574T=
ENST00000566510.5:c.*1169T= ENSP00000458139.1:n.*1169T=
ENST00000566612.5:c.*743T= ENSP00000454782.1:n.*743T=
ENST00000611625.4:c.2566T= ENSP00000481063.1:p.Tyr856=
ENST00000612417.4:c.1854-838T= ENSP00000478360.1:n.1854-838T=
ENST00000621016.4:c.1866-850T= ENSP00000480664.1:n.1866-850T=
NM_004360.3:c.2503T= , LRG_301t1:c.2503T= NP_004351.1:p.Tyr835=
XM_011523488.1:c.1768T= XP_011521790.1:p.Tyr590=
XM_011523489.1:c.1768T= XP_011521791.1:p.Tyr590=
NM_001317184.1:c.2320T= NP_001304113.1:p.Tyr774=
NM_001317185.1:c.955T= NP_001304114.1:p.Tyr319=
NM_001317186.1:c.538T= NP_001304115.1:p.Tyr180=
NM_004360.4:c.2503T= NP_004351.1:p.Tyr835=
NM_004360.5:c.2503T= MANE Select NP_004351.1:p.Tyr835=
NM_001317184.2:c.2320T= NP_001304113.1:p.Tyr774=
NM_001317185.2:c.955T= NP_001304114.1:p.Tyr319=
NM_001317186.2:c.538T= NP_001304115.1:p.Tyr180=