Canonical Allele Identifier: CA2229988763

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68827698C= , CM000678.2:g.68827698C=	GRCh38
NC_000016.9:g.68861601C= , CM000678.1:g.68861601C=	GRCh37
NC_000016.8:g.67419102C=	NCBI36
NG_008021.1:g.95407C= , LRG_301:g.95407C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2165-476C= MANE Select	ENSP00000261769.4:n.2165-476C=
ENST00000261769.9:c.2165-476C=	ENSP00000261769.4:n.2165-476C=
ENST00000422392.6:c.1982-476C=	ENSP00000414946.2:n.1982-476C=
ENST00000562118.1:n.383-476C=
ENST00000562836.5:n.2236-476C=
ENST00000566510.5:c.*831-476C=	ENSP00000458139.1:n.*831-476C=
ENST00000566612.5:c.*405-476C=	ENSP00000454782.1:n.*405-476C=
ENST00000611625.4:c.2228-476C=	ENSP00000481063.1:n.2228-476C=
ENST00000612417.4:c.1853+1144C=	ENSP00000478360.1:n.1853+1144C=
ENST00000621016.4:c.1865+5544C=	ENSP00000480664.1:n.1865+5544C=
NM_004360.3:c.2165-476C= , LRG_301t1:c.2165-476C=	NP_004351.1:n.2165-476C=
XM_011523488.1:c.1430-476C=	XP_011521790.1:n.1430-476C=
XM_011523489.1:c.1430-476C=	XP_011521791.1:n.1430-476C=
NM_001317184.1:c.1982-476C=	NP_001304113.1:n.1982-476C=
NM_001317185.1:c.617-476C=	NP_001304114.1:n.617-476C=
NM_001317186.1:c.200-476C=	NP_001304115.1:n.200-476C=
NM_004360.4:c.2165-476C=	NP_004351.1:n.2165-476C=
NM_004360.5:c.2165-476C= MANE Select	NP_004351.1:n.2165-476C=
NM_001317184.2:c.1982-476C=	NP_001304113.1:n.1982-476C=
NM_001317185.2:c.617-476C=	NP_001304114.1:n.617-476C=
NM_001317186.2:c.200-476C=	NP_001304115.1:n.200-476C=