Canonical Allele Identifier: CA2229978494

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833459A= , CM000678.2:g.68833459A=	GRCh38
NC_000016.9:g.68867362A= , CM000678.1:g.68867362A=	GRCh37
NC_000016.8:g.67424863A=	NCBI36
NG_008021.1:g.101168A= , LRG_301:g.101168A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2609A= MANE Select	ENSP00000261769.4:p.Lys870=
ENST00000261769.9:c.2609A=	ENSP00000261769.4:p.Lys870=
ENST00000422392.6:c.2426A=	ENSP00000414946.2:p.Lys809=
ENST00000562118.1:n.827A=
ENST00000562836.5:n.2680A=
ENST00000566510.5:c.*1275A=	ENSP00000458139.1:n.*1275A=
ENST00000566612.5:c.*849A=	ENSP00000454782.1:n.*849A=
ENST00000611625.4:c.2672A=	ENSP00000481063.1:p.Lys891=
ENST00000612417.4:c.1854-732A=	ENSP00000478360.1:n.1854-732A=
ENST00000621016.4:c.1866-744A=	ENSP00000480664.1:n.1866-744A=
NM_004360.3:c.2609A= , LRG_301t1:c.2609A=	NP_004351.1:p.Lys870=
XM_011523488.1:c.1874A=	XP_011521790.1:p.Lys625=
XM_011523489.1:c.1874A=	XP_011521791.1:p.Lys625=
NM_001317184.1:c.2426A=	NP_001304113.1:p.Lys809=
NM_001317185.1:c.1061A=	NP_001304114.1:p.Lys354=
NM_001317186.1:c.644A=	NP_001304115.1:p.Lys215=
NM_004360.4:c.2609A=	NP_004351.1:p.Lys870=
NM_004360.5:c.2609A= MANE Select	NP_004351.1:p.Lys870=
NM_001317184.2:c.2426A=	NP_001304113.1:p.Lys809=
NM_001317185.2:c.1061A=	NP_001304114.1:p.Lys354=
NM_001317186.2:c.644A=	NP_001304115.1:p.Lys215=