Canonical Allele Identifier: CA2229978459

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833445G= , CM000678.2:g.68833445G=	GRCh38
NC_000016.9:g.68867348G= , CM000678.1:g.68867348G=	GRCh37
NC_000016.8:g.67424849G=	NCBI36
NG_008021.1:g.101154G= , LRG_301:g.101154G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2595G= MANE Select	ENSP00000261769.4:p.Trp865=
ENST00000261769.9:c.2595G=	ENSP00000261769.4:p.Trp865=
ENST00000422392.6:c.2412G=	ENSP00000414946.2:p.Trp804=
ENST00000562118.1:n.813G=
ENST00000562836.5:n.2666G=
ENST00000566510.5:c.*1261G=	ENSP00000458139.1:n.*1261G=
ENST00000566612.5:c.*835G=	ENSP00000454782.1:n.*835G=
ENST00000611625.4:c.2658G=	ENSP00000481063.1:p.Trp886=
ENST00000612417.4:c.1854-746G=	ENSP00000478360.1:n.1854-746G=
ENST00000621016.4:c.1866-758G=	ENSP00000480664.1:n.1866-758G=
NM_004360.3:c.2595G= , LRG_301t1:c.2595G=	NP_004351.1:p.Trp865=
XM_011523488.1:c.1860G=	XP_011521790.1:p.Trp620=
XM_011523489.1:c.1860G=	XP_011521791.1:p.Trp620=
NM_001317184.1:c.2412G=	NP_001304113.1:p.Trp804=
NM_001317185.1:c.1047G=	NP_001304114.1:p.Trp349=
NM_001317186.1:c.630G=	NP_001304115.1:p.Trp210=
NM_004360.4:c.2595G=	NP_004351.1:p.Trp865=
NM_004360.5:c.2595G= MANE Select	NP_004351.1:p.Trp865=
NM_001317184.2:c.2412G=	NP_001304113.1:p.Trp804=
NM_001317185.2:c.1047G=	NP_001304114.1:p.Trp349=
NM_001317186.2:c.630G=	NP_001304115.1:p.Trp210=