Canonical Allele Identifier: CA2229980482

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822068C= , CM000678.2:g.68822068C=	GRCh38
NC_000016.9:g.68855971C= , CM000678.1:g.68855971C=	GRCh37
NC_000016.8:g.67413472C=	NCBI36
NG_008021.1:g.89777C= , LRG_301:g.89777C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1779C= MANE Select	ENSP00000261769.4:p.Pro593=
ENST00000261769.9:c.1779C=	ENSP00000261769.4:p.Pro593=
ENST00000422392.6:c.1596C=	ENSP00000414946.2:p.Pro532=
ENST00000562836.5:n.1850C=
ENST00000566510.5:c.*445C=	ENSP00000458139.1:n.*445C=
ENST00000566612.5:c.*19C=	ENSP00000454782.1:n.*19C=
ENST00000611625.4:c.1842C=	ENSP00000481063.1:p.Pro614=
ENST00000612417.4:c.1779C=	ENSP00000478360.1:p.Pro593=
ENST00000621016.4:c.1779C=	ENSP00000480664.1:p.Pro593=
NM_004360.3:c.1779C= , LRG_301t1:c.1779C=	NP_004351.1:p.Pro593=
XM_011523488.1:c.1044C=	XP_011521790.1:p.Pro348=
XM_011523489.1:c.1044C=	XP_011521791.1:p.Pro348=
NM_001317184.1:c.1596C=	NP_001304113.1:p.Pro532=
NM_001317185.1:c.231C=	NP_001304114.1:p.Pro77=
NM_001317186.1:c.-187C=	NP_001304115.1:n.-187C=
NM_004360.4:c.1779C=	NP_004351.1:p.Pro593=
NM_004360.5:c.1779C= MANE Select	NP_004351.1:p.Pro593=
NM_001317184.2:c.1596C=	NP_001304113.1:p.Pro532=
NM_001317185.2:c.231C=	NP_001304114.1:p.Pro77=
NM_001317186.2:c.-187C=	NP_001304115.1:n.-187C=