Canonical Allele Identifier: CA2229967466

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810473A= , CM000678.2:g.68810473A=	GRCh38
NC_000016.9:g.68844376A= , CM000678.1:g.68844376A=	GRCh37
NC_000016.8:g.67401877A=	NCBI36
NG_008021.1:g.78182A= , LRG_301:g.78182A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.832+132A= MANE Select	ENSP00000261769.4:n.832+132A=
ENST00000261769.9:c.832+132A=	ENSP00000261769.4:n.832+132A=
ENST00000422392.6:c.832+132A=	ENSP00000414946.2:n.832+132A=
ENST00000561751.1:c.455-1211A=
ENST00000562836.5:n.903+132A=
ENST00000566510.5:c.676+132A=	ENSP00000458139.1:n.676+132A=
ENST00000566612.5:c.832+132A=	ENSP00000454782.1:n.832+132A=
ENST00000611625.4:c.832+132A=	ENSP00000481063.1:n.832+132A=
ENST00000612417.4:c.832+132A=	ENSP00000478360.1:n.832+132A=
ENST00000621016.4:c.832+132A=	ENSP00000480664.1:n.832+132A=
NM_004360.3:c.832+132A= , LRG_301t1:c.832+132A=	NP_004351.1:n.832+132A=
XM_011523488.1:c.97+132A=	XP_011521790.1:n.97+132A=
XM_011523489.1:c.97+132A=	XP_011521791.1:n.97+132A=
NM_001317184.1:c.832+132A=	NP_001304113.1:n.832+132A=
NM_001317185.1:c.-784+132A=	NP_001304114.1:n.-784+132A=
NM_001317186.1:c.-988+132A=	NP_001304115.1:n.-988+132A=
NM_004360.4:c.832+132A=	NP_004351.1:n.832+132A=
NM_004360.5:c.832+132A= MANE Select	NP_004351.1:n.832+132A=
NM_001317184.2:c.832+132A=	NP_001304113.1:n.832+132A=
NM_001317185.2:c.-784+132A=	NP_001304114.1:n.-784+132A=
NM_001317186.2:c.-988+132A=	NP_001304115.1:n.-988+132A=