Canonical Allele Identifier: CA2229981551

Gene: CDH1 FTLP14

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822714A= , CM000678.2:g.68822714A=	GRCh38
NC_000016.9:g.68856617A= , CM000678.1:g.68856617A=	GRCh37
NC_000016.8:g.67414118A=	NCBI36
NG_008021.1:g.90423A= , LRG_301:g.90423A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1936+489A= (CDH1) MANE Select	ENSP00000261769.4:n.1936+489A=
ENST00000261769.9:c.1936+489A= (CDH1)	ENSP00000261769.4:n.1936+489A=
ENST00000422392.6:c.1753+489A= (CDH1)	ENSP00000414946.2:n.1753+489A=
ENST00000562087.2:n.128A= (FTLP14)
ENST00000562836.5:n.2007+489A= (CDH1)
ENST00000566510.5:c.*602+489A= (CDH1)	ENSP00000458139.1:n.*602+489A=
ENST00000566612.5:c.*176+489A= (CDH1)	ENSP00000454782.1:n.*176+489A=
ENST00000611625.4:c.1999+489A= (CDH1)	ENSP00000481063.1:n.1999+489A=
ENST00000612417.4:c.1830+595A= (CDH1)	ENSP00000478360.1:n.1830+595A=
ENST00000621016.4:c.1865+560A= (CDH1)	ENSP00000480664.1:n.1865+560A=
NM_004360.3:c.1936+489A= , LRG_301t1:c.1936+489A= (CDH1)	NP_004351.1:n.1936+489A=
XM_011523488.1:c.1201+489A= (CDH1)	XP_011521790.1:n.1201+489A=
XM_011523489.1:c.1201+489A= (CDH1)	XP_011521791.1:n.1201+489A=
NM_001317184.1:c.1753+489A= (CDH1)	NP_001304113.1:n.1753+489A=
NM_001317185.1:c.388+489A= (CDH1)	NP_001304114.1:n.388+489A=
NM_001317186.1:c.-30+489A= (CDH1)	NP_001304115.1:n.-30+489A=
NM_004360.4:c.1936+489A= (CDH1)	NP_004351.1:n.1936+489A=
NM_004360.5:c.1936+489A= (CDH1) MANE Select	NP_004351.1:n.1936+489A=
NM_001317184.2:c.1753+489A= (CDH1)	NP_001304113.1:n.1753+489A=
NM_001317185.2:c.388+489A= (CDH1)	NP_001304114.1:n.388+489A=
NM_001317186.2:c.-30+489A= (CDH1)	NP_001304115.1:n.-30+489A=