Canonical Allele Identifier: CA2229978346
Gene: CDH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819715G= , CM000678.2:g.68819715G= GRCh38
NC_000016.9:g.68853618G= , CM000678.1:g.68853618G= GRCh37
NC_000016.8:g.67411119G= NCBI36
NG_008021.1:g.87424G= , LRG_301:g.87424G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1711+290G= MANE Select ENSP00000261769.4:n.1711+290G=
ENST00000261769.9:c.1711+290G= ENSP00000261769.4:n.1711+290G=
ENST00000422392.6:c.1528+290G= ENSP00000414946.2:n.1528+290G=
ENST00000562836.5:n.1782+290G=
ENST00000566510.5:c.*377+290G= ENSP00000458139.1:n.*377+290G=
ENST00000566612.5:c.1566-2286G= ENSP00000454782.1:n.1566-2286G=
ENST00000611625.4:c.1774+290G= ENSP00000481063.1:n.1774+290G=
ENST00000612417.4:c.1711+290G= ENSP00000478360.1:n.1711+290G=
ENST00000621016.4:c.1711+290G= ENSP00000480664.1:n.1711+290G=
NM_004360.3:c.1711+290G= , LRG_301t1:c.1711+290G= NP_004351.1:n.1711+290G=
XM_011523488.1:c.976+290G= XP_011521790.1:n.976+290G=
XM_011523489.1:c.976+290G= XP_011521791.1:n.976+290G=
NM_001317184.1:c.1528+290G= NP_001304113.1:n.1528+290G=
NM_001317185.1:c.163+290G= NP_001304114.1:n.163+290G=
NM_001317186.1:c.-254-2286G= NP_001304115.1:n.-254-2286G=
NM_004360.4:c.1711+290G= NP_004351.1:n.1711+290G=
NM_004360.5:c.1711+290G= MANE Select NP_004351.1:n.1711+290G=
NM_001317184.2:c.1528+290G= NP_001304113.1:n.1528+290G=
NM_001317185.2:c.163+290G= NP_001304114.1:n.163+290G=
NM_001317186.2:c.-254-2286G= NP_001304115.1:n.-254-2286G=
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