Canonical Allele Identifier: CA2229981758

Gene: CDH1 FTLP14

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822907C= , CM000678.2:g.68822907C=	GRCh38
NC_000016.9:g.68856810C= , CM000678.1:g.68856810C=	GRCh37
NC_000016.8:g.67414311C=	NCBI36
NG_008021.1:g.90616C= , LRG_301:g.90616C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1937-492C= (CDH1) MANE Select	ENSP00000261769.4:n.1937-492C=
ENST00000261769.9:c.1937-492C= (CDH1)	ENSP00000261769.4:n.1937-492C=
ENST00000422392.6:c.1754-492C= (CDH1)	ENSP00000414946.2:n.1754-492C=
ENST00000562087.2:n.321C= (FTLP14)
ENST00000562836.5:n.2008-492C= (CDH1)
ENST00000566510.5:c.*603-492C= (CDH1)	ENSP00000458139.1:n.*603-492C=
ENST00000566612.5:c.*177-492C= (CDH1)	ENSP00000454782.1:n.*177-492C=
ENST00000611625.4:c.2000-492C= (CDH1)	ENSP00000481063.1:n.2000-492C=
ENST00000612417.4:c.1830+788C= (CDH1)	ENSP00000478360.1:n.1830+788C=
ENST00000621016.4:c.1865+753C= (CDH1)	ENSP00000480664.1:n.1865+753C=
NM_004360.3:c.1937-492C= , LRG_301t1:c.1937-492C= (CDH1)	NP_004351.1:n.1937-492C=
XM_011523488.1:c.1202-492C= (CDH1)	XP_011521790.1:n.1202-492C=
XM_011523489.1:c.1202-492C= (CDH1)	XP_011521791.1:n.1202-492C=
NM_001317184.1:c.1754-492C= (CDH1)	NP_001304113.1:n.1754-492C=
NM_001317185.1:c.389-492C= (CDH1)	NP_001304114.1:n.389-492C=
NM_001317186.1:c.-29-492C= (CDH1)	NP_001304115.1:n.-29-492C=
NM_004360.4:c.1937-492C= (CDH1)	NP_004351.1:n.1937-492C=
NM_004360.5:c.1937-492C= (CDH1) MANE Select	NP_004351.1:n.1937-492C=
NM_001317184.2:c.1754-492C= (CDH1)	NP_001304113.1:n.1754-492C=
NM_001317185.2:c.389-492C= (CDH1)	NP_001304114.1:n.389-492C=
NM_001317186.2:c.-29-492C= (CDH1)	NP_001304115.1:n.-29-492C=