Canonical Allele Identifier: CA2229978350

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833412C= , CM000678.2:g.68833412C=	GRCh38
NC_000016.9:g.68867315C= , CM000678.1:g.68867315C=	GRCh37
NC_000016.8:g.67424816C=	NCBI36
NG_008021.1:g.101121C= , LRG_301:g.101121C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2562C= MANE Select	ENSP00000261769.4:p.Asp854=
ENST00000261769.9:c.2562C=	ENSP00000261769.4:p.Asp854=
ENST00000422392.6:c.2379C=	ENSP00000414946.2:p.Asp793=
ENST00000562118.1:n.780C=
ENST00000562836.5:n.2633C=
ENST00000566510.5:c.*1228C=	ENSP00000458139.1:n.*1228C=
ENST00000566612.5:c.*802C=	ENSP00000454782.1:n.*802C=
ENST00000611625.4:c.2625C=	ENSP00000481063.1:p.Asp875=
ENST00000612417.4:c.1854-779C=	ENSP00000478360.1:n.1854-779C=
ENST00000621016.4:c.1866-791C=	ENSP00000480664.1:n.1866-791C=
NM_004360.3:c.2562C= , LRG_301t1:c.2562C=	NP_004351.1:p.Asp854=
XM_011523488.1:c.1827C=	XP_011521790.1:p.Asp609=
XM_011523489.1:c.1827C=	XP_011521791.1:p.Asp609=
NM_001317184.1:c.2379C=	NP_001304113.1:p.Asp793=
NM_001317185.1:c.1014C=	NP_001304114.1:p.Asp338=
NM_001317186.1:c.597C=	NP_001304115.1:p.Asp199=
NM_004360.4:c.2562C=	NP_004351.1:p.Asp854=
NM_004360.5:c.2562C= MANE Select	NP_004351.1:p.Asp854=
NM_001317184.2:c.2379C=	NP_001304113.1:p.Asp793=
NM_001317185.2:c.1014C=	NP_001304114.1:p.Asp338=
NM_001317186.2:c.597C=	NP_001304115.1:p.Asp199=