Canonical Allele Identifier: CA2229978328
Gene: CDH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819690C= , CM000678.2:g.68819690C= GRCh38
NC_000016.9:g.68853593C= , CM000678.1:g.68853593C= GRCh37
NC_000016.8:g.67411094C= NCBI36
NG_008021.1:g.87399C= , LRG_301:g.87399C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1711+265C= MANE Select ENSP00000261769.4:n.1711+265C=
ENST00000261769.9:c.1711+265C= ENSP00000261769.4:n.1711+265C=
ENST00000422392.6:c.1528+265C= ENSP00000414946.2:n.1528+265C=
ENST00000562836.5:n.1782+265C=
ENST00000566510.5:c.*377+265C= ENSP00000458139.1:n.*377+265C=
ENST00000566612.5:c.1566-2311C= ENSP00000454782.1:n.1566-2311C=
ENST00000611625.4:c.1774+265C= ENSP00000481063.1:n.1774+265C=
ENST00000612417.4:c.1711+265C= ENSP00000478360.1:n.1711+265C=
ENST00000621016.4:c.1711+265C= ENSP00000480664.1:n.1711+265C=
NM_004360.3:c.1711+265C= , LRG_301t1:c.1711+265C= NP_004351.1:n.1711+265C=
XM_011523488.1:c.976+265C= XP_011521790.1:n.976+265C=
XM_011523489.1:c.976+265C= XP_011521791.1:n.976+265C=
NM_001317184.1:c.1528+265C= NP_001304113.1:n.1528+265C=
NM_001317185.1:c.163+265C= NP_001304114.1:n.163+265C=
NM_001317186.1:c.-254-2311C= NP_001304115.1:n.-254-2311C=
NM_004360.4:c.1711+265C= NP_004351.1:n.1711+265C=
NM_004360.5:c.1711+265C= MANE Select NP_004351.1:n.1711+265C=
NM_001317184.2:c.1528+265C= NP_001304113.1:n.1528+265C=
NM_001317185.2:c.163+265C= NP_001304114.1:n.163+265C=
NM_001317186.2:c.-254-2311C= NP_001304115.1:n.-254-2311C=
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