Canonical Allele Identifier: CA2229978712
Gene: CDH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833518G= , CM000678.2:g.68833518G= GRCh38
NC_000016.9:g.68867421G= , CM000678.1:g.68867421G= GRCh37
NC_000016.8:g.67424922G= NCBI36
NG_008021.1:g.101227G= , LRG_301:g.101227G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.*19G= MANE Select ENSP00000261769.4:n.*19G=
ENST00000261769.9:c.*19G= ENSP00000261769.4:n.*19G=
ENST00000422392.6:c.*19G= ENSP00000414946.2:n.*19G=
ENST00000562118.1:n.886G=
ENST00000562836.5:n.2739G=
ENST00000566510.5:c.*1334G= ENSP00000458139.1:n.*1334G=
ENST00000566612.5:c.*908G= ENSP00000454782.1:n.*908G=
ENST00000611625.4:c.*19G= ENSP00000481063.1:n.*19G=
ENST00000612417.4:c.1854-673G= ENSP00000478360.1:n.1854-673G=
ENST00000621016.4:c.1866-685G= ENSP00000480664.1:n.1866-685G=
NM_004360.3:c.*19G= , LRG_301t1:c.*19G= NP_004351.1:n.*19G=
XM_011523488.1:c.*19G= XP_011521790.1:n.*19G=
XM_011523489.1:c.*19G= XP_011521791.1:n.*19G=
NM_001317184.1:c.*19G= NP_001304113.1:n.*19G=
NM_001317185.1:c.*19G= NP_001304114.1:n.*19G=
NM_001317186.1:c.*19G= NP_001304115.1:n.*19G=
NM_004360.4:c.*19G= NP_004351.1:n.*19G=
NM_004360.5:c.*19G= MANE Select NP_004351.1:n.*19G=
NM_001317184.2:c.*19G= NP_001304113.1:n.*19G=
NM_001317185.2:c.*19G= NP_001304114.1:n.*19G=
NM_001317186.2:c.*19G= NP_001304115.1:n.*19G=
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