Canonical Allele Identifier: CA2229980494

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822072C= , CM000678.2:g.68822072C=	GRCh38
NC_000016.9:g.68855975C= , CM000678.1:g.68855975C=	GRCh37
NC_000016.8:g.67413476C=	NCBI36
NG_008021.1:g.89781C= , LRG_301:g.89781C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1783C= MANE Select	ENSP00000261769.4:p.Pro595=
ENST00000261769.9:c.1783C=	ENSP00000261769.4:p.Pro595=
ENST00000422392.6:c.1600C=	ENSP00000414946.2:p.Pro534=
ENST00000562836.5:n.1854C=
ENST00000566510.5:c.*449C=	ENSP00000458139.1:n.*449C=
ENST00000566612.5:c.*23C=	ENSP00000454782.1:n.*23C=
ENST00000611625.4:c.1846C=	ENSP00000481063.1:p.Pro616=
ENST00000612417.4:c.1783C=	ENSP00000478360.1:p.Pro595=
ENST00000621016.4:c.1783C=	ENSP00000480664.1:p.Pro595=
NM_004360.3:c.1783C= , LRG_301t1:c.1783C=	NP_004351.1:p.Pro595=
XM_011523488.1:c.1048C=	XP_011521790.1:p.Pro350=
XM_011523489.1:c.1048C=	XP_011521791.1:p.Pro350=
NM_001317184.1:c.1600C=	NP_001304113.1:p.Pro534=
NM_001317185.1:c.235C=	NP_001304114.1:p.Pro79=
NM_001317186.1:c.-183C=	NP_001304115.1:n.-183C=
NM_004360.4:c.1783C=	NP_004351.1:p.Pro595=
NM_004360.5:c.1783C= MANE Select	NP_004351.1:p.Pro595=
NM_001317184.2:c.1600C=	NP_001304113.1:p.Pro534=
NM_001317185.2:c.235C=	NP_001304114.1:p.Pro79=
NM_001317186.2:c.-183C=	NP_001304115.1:n.-183C=