Canonical Allele Identifier: CA2229978776
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833585G= , CM000678.2:g.68833585G= GRCh38
NC_000016.9:g.68867488G= , CM000678.1:g.68867488G= GRCh37
NC_000016.8:g.67424989G= NCBI36
NG_008021.1:g.101294G= , LRG_301:g.101294G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.*86G= MANE Select ENSP00000261769.4:n.*86G=
ENST00000261769.9:c.*86G= ENSP00000261769.4:n.*86G=
ENST00000566612.5:c.*975G= ENSP00000454782.1:n.*975G=
ENST00000611625.4:c.*86G= ENSP00000481063.1:n.*86G=
ENST00000612417.4:c.1854-606G= ENSP00000478360.1:n.1854-606G=
ENST00000621016.4:c.1866-618G= ENSP00000480664.1:n.1866-618G=
NM_004360.3:c.*86G= , LRG_301t1:c.*86G= NP_004351.1:n.*86G=
XM_011523488.1:c.*86G= XP_011521790.1:n.*86G=
XM_011523489.1:c.*86G= XP_011521791.1:n.*86G=
NM_001317184.1:c.*86G= NP_001304113.1:n.*86G=
NM_001317185.1:c.*86G= NP_001304114.1:n.*86G=
NM_001317186.1:c.*86G= NP_001304115.1:n.*86G=
NM_004360.4:c.*86G= NP_004351.1:n.*86G=
NM_004360.5:c.*86G= MANE Select NP_004351.1:n.*86G=
NM_001317184.2:c.*86G= NP_001304113.1:n.*86G=
NM_001317185.2:c.*86G= NP_001304114.1:n.*86G=
NM_001317186.2:c.*86G= NP_001304115.1:n.*86G=