Canonical Allele Identifier: CA2229978741
Gene: CDH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833537G= , CM000678.2:g.68833537G= GRCh38
NC_000016.9:g.68867440G= , CM000678.1:g.68867440G= GRCh37
NC_000016.8:g.67424941G= NCBI36
NG_008021.1:g.101246G= , LRG_301:g.101246G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.*38G= MANE Select ENSP00000261769.4:n.*38G=
ENST00000261769.9:c.*38G= ENSP00000261769.4:n.*38G=
ENST00000562118.1:n.905G=
ENST00000562836.5:n.2758G=
ENST00000566612.5:c.*927G= ENSP00000454782.1:n.*927G=
ENST00000611625.4:c.*38G= ENSP00000481063.1:n.*38G=
ENST00000612417.4:c.1854-654G= ENSP00000478360.1:n.1854-654G=
ENST00000621016.4:c.1866-666G= ENSP00000480664.1:n.1866-666G=
NM_004360.3:c.*38G= , LRG_301t1:c.*38G= NP_004351.1:n.*38G=
XM_011523488.1:c.*38G= XP_011521790.1:n.*38G=
XM_011523489.1:c.*38G= XP_011521791.1:n.*38G=
NM_001317184.1:c.*38G= NP_001304113.1:n.*38G=
NM_001317185.1:c.*38G= NP_001304114.1:n.*38G=
NM_001317186.1:c.*38G= NP_001304115.1:n.*38G=
NM_004360.4:c.*38G= NP_004351.1:n.*38G=
NM_004360.5:c.*38G= MANE Select NP_004351.1:n.*38G=
NM_001317184.2:c.*38G= NP_001304113.1:n.*38G=
NM_001317185.2:c.*38G= NP_001304114.1:n.*38G=
NM_001317186.2:c.*38G= NP_001304115.1:n.*38G=
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