Canonical Allele Identifier: CA2229967279

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810332G= , CM000678.2:g.68810332G=	GRCh38
NC_000016.9:g.68844235G= , CM000678.1:g.68844235G=	GRCh37
NC_000016.8:g.67401736G=	NCBI36
NG_008021.1:g.78041G= , LRG_301:g.78041G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.823G= MANE Select	ENSP00000261769.4:p.Ala275=
ENST00000261769.9:c.823G=	ENSP00000261769.4:p.Ala275=
ENST00000422392.6:c.823G=	ENSP00000414946.2:p.Ala275=
ENST00000561751.1:c.455-1352G=
ENST00000562836.5:n.894G=
ENST00000566510.5:c.667G=	ENSP00000458139.1:p.Ala223=
ENST00000566612.5:c.823G=	ENSP00000454782.1:p.Ala275=
ENST00000611625.4:c.823G=	ENSP00000481063.1:p.Ala275=
ENST00000612417.4:c.823G=	ENSP00000478360.1:p.Ala275=
ENST00000621016.4:c.823G=	ENSP00000480664.1:p.Ala275=
NM_004360.3:c.823G= , LRG_301t1:c.823G=	NP_004351.1:p.Ala275=
XM_011523488.1:c.88G=	XP_011521790.1:p.Ala30=
XM_011523489.1:c.88G=	XP_011521791.1:p.Ala30=
NM_001317184.1:c.823G=	NP_001304113.1:p.Ala275=
NM_001317185.1:c.-793G=	NP_001304114.1:n.-793G=
NM_001317186.1:c.-997G=	NP_001304115.1:n.-997G=
NM_004360.4:c.823G=	NP_004351.1:p.Ala275=
NM_004360.5:c.823G= MANE Select	NP_004351.1:p.Ala275=
NM_001317184.2:c.823G=	NP_001304113.1:p.Ala275=
NM_001317185.2:c.-793G=	NP_001304114.1:n.-793G=
NM_001317186.2:c.-997G=	NP_001304115.1:n.-997G=