Canonical Allele Identifier: CA2229978149
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833336C= , CM000678.2:g.68833336C= GRCh38
NC_000016.9:g.68867239C= , CM000678.1:g.68867239C= GRCh37
NC_000016.8:g.67424740C= NCBI36
NG_008021.1:g.101045C= , LRG_301:g.101045C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2486C= MANE Select ENSP00000261769.4:p.Ser829=
ENST00000261769.9:c.2486C= ENSP00000261769.4:p.Ser829=
ENST00000422392.6:c.2303C= ENSP00000414946.2:p.Ser768=
ENST00000562118.1:n.704C=
ENST00000562836.5:n.2557C=
ENST00000566510.5:c.*1152C= ENSP00000458139.1:n.*1152C=
ENST00000566612.5:c.*726C= ENSP00000454782.1:n.*726C=
ENST00000611625.4:c.2549C= ENSP00000481063.1:p.Ser850=
ENST00000612417.4:c.1854-855C= ENSP00000478360.1:n.1854-855C=
ENST00000621016.4:c.1866-867C= ENSP00000480664.1:n.1866-867C=
NM_004360.3:c.2486C= , LRG_301t1:c.2486C= NP_004351.1:p.Ser829=
XM_011523488.1:c.1751C= XP_011521790.1:p.Ser584=
XM_011523489.1:c.1751C= XP_011521791.1:p.Ser584=
NM_001317184.1:c.2303C= NP_001304113.1:p.Ser768=
NM_001317185.1:c.938C= NP_001304114.1:p.Ser313=
NM_001317186.1:c.521C= NP_001304115.1:p.Ser174=
NM_004360.4:c.2486C= NP_004351.1:p.Ser829=
NM_004360.5:c.2486C= MANE Select NP_004351.1:p.Ser829=
NM_001317184.2:c.2303C= NP_001304113.1:p.Ser768=
NM_001317185.2:c.938C= NP_001304114.1:p.Ser313=
NM_001317186.2:c.521C= NP_001304115.1:p.Ser174=