Canonical Allele Identifier: CA2229992031

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829665G= , CM000678.2:g.68829665G=	GRCh38
NC_000016.9:g.68863568G= , CM000678.1:g.68863568G=	GRCh37
NC_000016.8:g.67421069G=	NCBI36
NG_008021.1:g.97374G= , LRG_301:g.97374G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2307G= MANE Select	ENSP00000261769.4:p.Leu769=
ENST00000261769.9:c.2307G=	ENSP00000261769.4:p.Leu769=
ENST00000422392.6:c.2124G=	ENSP00000414946.2:p.Leu708=
ENST00000562118.1:n.525G=
ENST00000562836.5:n.2378G=
ENST00000566510.5:c.*973G=	ENSP00000458139.1:n.*973G=
ENST00000566612.5:c.*547G=	ENSP00000454782.1:n.*547G=
ENST00000611625.4:c.2370G=	ENSP00000481063.1:p.Leu790=
ENST00000612417.4:c.1853+3111G=	ENSP00000478360.1:n.1853+3111G=
ENST00000621016.4:c.1866-4538G=	ENSP00000480664.1:n.1866-4538G=
NM_004360.3:c.2307G= , LRG_301t1:c.2307G=	NP_004351.1:p.Leu769=
XM_011523488.1:c.1572G=	XP_011521790.1:p.Leu524=
XM_011523489.1:c.1572G=	XP_011521791.1:p.Leu524=
NM_001317184.1:c.2124G=	NP_001304113.1:p.Leu708=
NM_001317185.1:c.759G=	NP_001304114.1:p.Leu253=
NM_001317186.1:c.342G=	NP_001304115.1:p.Leu114=
NM_004360.4:c.2307G=	NP_004351.1:p.Leu769=
NM_004360.5:c.2307G= MANE Select	NP_004351.1:p.Leu769=
NM_001317184.2:c.2124G=	NP_001304113.1:p.Leu708=
NM_001317185.2:c.759G=	NP_001304114.1:p.Leu253=
NM_001317186.2:c.342G=	NP_001304115.1:p.Leu114=