Canonical Allele Identifier: CA2229978231

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833383C= , CM000678.2:g.68833383C=	GRCh38
NC_000016.9:g.68867286C= , CM000678.1:g.68867286C=	GRCh37
NC_000016.8:g.67424787C=	NCBI36
NG_008021.1:g.101092C= , LRG_301:g.101092C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2533C= MANE Select	ENSP00000261769.4:p.Leu845=
ENST00000261769.9:c.2533C=	ENSP00000261769.4:p.Leu845=
ENST00000422392.6:c.2350C=	ENSP00000414946.2:p.Leu784=
ENST00000562118.1:n.751C=
ENST00000562836.5:n.2604C=
ENST00000566510.5:c.*1199C=	ENSP00000458139.1:n.*1199C=
ENST00000566612.5:c.*773C=	ENSP00000454782.1:n.*773C=
ENST00000611625.4:c.2596C=	ENSP00000481063.1:p.Leu866=
ENST00000612417.4:c.1854-808C=	ENSP00000478360.1:n.1854-808C=
ENST00000621016.4:c.1866-820C=	ENSP00000480664.1:n.1866-820C=
NM_004360.3:c.2533C= , LRG_301t1:c.2533C=	NP_004351.1:p.Leu845=
XM_011523488.1:c.1798C=	XP_011521790.1:p.Leu600=
XM_011523489.1:c.1798C=	XP_011521791.1:p.Leu600=
NM_001317184.1:c.2350C=	NP_001304113.1:p.Leu784=
NM_001317185.1:c.985C=	NP_001304114.1:p.Leu329=
NM_001317186.1:c.568C=	NP_001304115.1:p.Leu190=
NM_004360.4:c.2533C=	NP_004351.1:p.Leu845=
NM_004360.5:c.2533C= MANE Select	NP_004351.1:p.Leu845=
NM_001317184.2:c.2350C=	NP_001304113.1:p.Leu784=
NM_001317185.2:c.985C=	NP_001304114.1:p.Leu329=
NM_001317186.2:c.568C=	NP_001304115.1:p.Leu190=