Canonical Allele Identifier: CA2229977450
Gene: CDH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819062A= , CM000678.2:g.68819062A= GRCh38
NC_000016.9:g.68852965A= , CM000678.1:g.68852965A= GRCh37
NC_000016.8:g.67410466A= NCBI36
NG_008021.1:g.86771A= , LRG_301:g.86771A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1566-218A= MANE Select ENSP00000261769.4:n.1566-218A=
ENST00000261769.9:c.1566-218A= ENSP00000261769.4:n.1566-218A=
ENST00000422392.6:c.1383-218A= ENSP00000414946.2:n.1383-218A=
ENST00000562836.5:n.1637-218A=
ENST00000566510.5:c.*232-218A= ENSP00000458139.1:n.*232-218A=
ENST00000566612.5:c.1566-2939A= ENSP00000454782.1:n.1566-2939A=
ENST00000611625.4:c.1629-218A= ENSP00000481063.1:n.1629-218A=
ENST00000612417.4:c.1566-218A= ENSP00000478360.1:n.1566-218A=
ENST00000621016.4:c.1566-218A= ENSP00000480664.1:n.1566-218A=
NM_004360.3:c.1566-218A= , LRG_301t1:c.1566-218A= NP_004351.1:n.1566-218A=
XM_011523488.1:c.831-218A= XP_011521790.1:n.831-218A=
XM_011523489.1:c.831-218A= XP_011521791.1:n.831-218A=
NM_001317184.1:c.1383-218A= NP_001304113.1:n.1383-218A=
NM_001317185.1:c.18-218A= NP_001304114.1:n.18-218A=
NM_001317186.1:c.-254-2939A= NP_001304115.1:n.-254-2939A=
NM_004360.4:c.1566-218A= NP_004351.1:n.1566-218A=
NM_004360.5:c.1566-218A= MANE Select NP_004351.1:n.1566-218A=
NM_001317184.2:c.1383-218A= NP_001304113.1:n.1383-218A=
NM_001317185.2:c.18-218A= NP_001304114.1:n.18-218A=
NM_001317186.2:c.-254-2939A= NP_001304115.1:n.-254-2939A=
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