Canonical Allele Identifier: CA2229981846

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68823016A= , CM000678.2:g.68823016A= GRCh38
NC_000016.9:g.68856919A= , CM000678.1:g.68856919A= GRCh37
NC_000016.8:g.67414420A= NCBI36
NG_008021.1:g.90725A= , LRG_301:g.90725A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1937-383A= (CDH1) MANE Select ENSP00000261769.4:n.1937-383A=
ENST00000261769.9:c.1937-383A= (CDH1) ENSP00000261769.4:n.1937-383A=
ENST00000422392.6:c.1754-383A= (CDH1) ENSP00000414946.2:n.1754-383A=
ENST00000562087.2:n.430A= (FTLP14)
ENST00000562836.5:n.2008-383A= (CDH1)
ENST00000566510.5:c.*603-383A= (CDH1) ENSP00000458139.1:n.*603-383A=
ENST00000566612.5:c.*177-383A= (CDH1) ENSP00000454782.1:n.*177-383A=
ENST00000611625.4:c.2000-383A= (CDH1) ENSP00000481063.1:n.2000-383A=
ENST00000612417.4:c.1830+897A= (CDH1) ENSP00000478360.1:n.1830+897A=
ENST00000621016.4:c.1865+862A= (CDH1) ENSP00000480664.1:n.1865+862A=
NM_004360.3:c.1937-383A= , LRG_301t1:c.1937-383A= (CDH1) NP_004351.1:n.1937-383A=
XM_011523488.1:c.1202-383A= (CDH1) XP_011521790.1:n.1202-383A=
XM_011523489.1:c.1202-383A= (CDH1) XP_011521791.1:n.1202-383A=
NM_001317184.1:c.1754-383A= (CDH1) NP_001304113.1:n.1754-383A=
NM_001317185.1:c.389-383A= (CDH1) NP_001304114.1:n.389-383A=
NM_001317186.1:c.-29-383A= (CDH1) NP_001304115.1:n.-29-383A=
NM_004360.4:c.1937-383A= (CDH1) NP_004351.1:n.1937-383A=
NM_004360.5:c.1937-383A= (CDH1) MANE Select NP_004351.1:n.1937-383A=
NM_001317184.2:c.1754-383A= (CDH1) NP_001304113.1:n.1754-383A=
NM_001317185.2:c.389-383A= (CDH1) NP_001304114.1:n.389-383A=
NM_001317186.2:c.-29-383A= (CDH1) NP_001304115.1:n.-29-383A=