Canonical Allele Identifier: CA2229975133

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829763C= , CM000678.2:g.68829763C=	GRCh38
NC_000016.9:g.68863666C= , CM000678.1:g.68863666C=	GRCh37
NC_000016.8:g.67421167C=	NCBI36
NG_008021.1:g.97472C= , LRG_301:g.97472C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2405C= MANE Select	ENSP00000261769.4:p.Ala802=
ENST00000261769.9:c.2405C=	ENSP00000261769.4:p.Ala802=
ENST00000422392.6:c.2222C=	ENSP00000414946.2:p.Ala741=
ENST00000562118.1:n.623C=
ENST00000562836.5:n.2476C=
ENST00000566510.5:c.*1071C=	ENSP00000458139.1:n.*1071C=
ENST00000566612.5:c.*645C=	ENSP00000454782.1:n.*645C=
ENST00000611625.4:c.2468C=	ENSP00000481063.1:p.Ala823=
ENST00000612417.4:c.1853+3209C=	ENSP00000478360.1:n.1853+3209C=
ENST00000621016.4:c.1866-4440C=	ENSP00000480664.1:n.1866-4440C=
NM_004360.3:c.2405C= , LRG_301t1:c.2405C=	NP_004351.1:p.Ala802=
XM_011523488.1:c.1670C=	XP_011521790.1:p.Ala557=
XM_011523489.1:c.1670C=	XP_011521791.1:p.Ala557=
NM_001317184.1:c.2222C=	NP_001304113.1:p.Ala741=
NM_001317185.1:c.857C=	NP_001304114.1:p.Ala286=
NM_001317186.1:c.440C=	NP_001304115.1:p.Ala147=
NM_004360.4:c.2405C=	NP_004351.1:p.Ala802=
NM_004360.5:c.2405C= MANE Select	NP_004351.1:p.Ala802=
NM_001317184.2:c.2222C=	NP_001304113.1:p.Ala741=
NM_001317185.2:c.857C=	NP_001304114.1:p.Ala286=
NM_001317186.2:c.440C=	NP_001304115.1:p.Ala147=