Canonical Allele Identifier: CA2229980438

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822061A= , CM000678.2:g.68822061A=	GRCh38
NC_000016.9:g.68855964A= , CM000678.1:g.68855964A=	GRCh37
NC_000016.8:g.67413465A=	NCBI36
NG_008021.1:g.89770A= , LRG_301:g.89770A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1772A= MANE Select	ENSP00000261769.4:p.Asn591=
ENST00000261769.9:c.1772A=	ENSP00000261769.4:p.Asn591=
ENST00000422392.6:c.1589A=	ENSP00000414946.2:p.Asn530=
ENST00000562836.5:n.1843A=
ENST00000566510.5:c.*438A=	ENSP00000458139.1:n.*438A=
ENST00000566612.5:c.*12A=	ENSP00000454782.1:n.*12A=
ENST00000611625.4:c.1835A=	ENSP00000481063.1:p.Asn612=
ENST00000612417.4:c.1772A=	ENSP00000478360.1:p.Asn591=
ENST00000621016.4:c.1772A=	ENSP00000480664.1:p.Asn591=
NM_004360.3:c.1772A= , LRG_301t1:c.1772A=	NP_004351.1:p.Asn591=
XM_011523488.1:c.1037A=	XP_011521790.1:p.Asn346=
XM_011523489.1:c.1037A=	XP_011521791.1:p.Asn346=
NM_001317184.1:c.1589A=	NP_001304113.1:p.Asn530=
NM_001317185.1:c.224A=	NP_001304114.1:p.Asn75=
NM_001317186.1:c.-194A=	NP_001304115.1:n.-194A=
NM_004360.4:c.1772A=	NP_004351.1:p.Asn591=
NM_004360.5:c.1772A= MANE Select	NP_004351.1:p.Asn591=
NM_001317184.2:c.1589A=	NP_001304113.1:p.Asn530=
NM_001317185.2:c.224A=	NP_001304114.1:p.Asn75=
NM_001317186.2:c.-194A=	NP_001304115.1:n.-194A=