Canonical Allele Identifier: CA2229975370

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829877T= , CM000678.2:g.68829877T=	GRCh38
NC_000016.9:g.68863780T= , CM000678.1:g.68863780T=	GRCh37
NC_000016.8:g.67421281T=	NCBI36
NG_008021.1:g.97586T= , LRG_301:g.97586T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2439+80T= MANE Select	ENSP00000261769.4:n.2439+80T=
ENST00000261769.9:c.2439+80T=	ENSP00000261769.4:n.2439+80T=
ENST00000422392.6:c.2256+80T=	ENSP00000414946.2:n.2256+80T=
ENST00000562118.1:n.657+80T=
ENST00000562836.5:n.2510+80T=
ENST00000566510.5:c.*1105+80T=	ENSP00000458139.1:n.*1105+80T=
ENST00000566612.5:c.*679+80T=	ENSP00000454782.1:n.*679+80T=
ENST00000611625.4:c.2502+80T=	ENSP00000481063.1:n.2502+80T=
ENST00000612417.4:c.1853+3323T=	ENSP00000478360.1:n.1853+3323T=
ENST00000621016.4:c.1866-4326T=	ENSP00000480664.1:n.1866-4326T=
NM_004360.3:c.2439+80T= , LRG_301t1:c.2439+80T=	NP_004351.1:n.2439+80T=
XM_011523488.1:c.1704+80T=	XP_011521790.1:n.1704+80T=
XM_011523489.1:c.1704+80T=	XP_011521791.1:n.1704+80T=
NM_001317184.1:c.2256+80T=	NP_001304113.1:n.2256+80T=
NM_001317185.1:c.891+80T=	NP_001304114.1:n.891+80T=
NM_001317186.1:c.474+80T=	NP_001304115.1:n.474+80T=
NM_004360.4:c.2439+80T=	NP_004351.1:n.2439+80T=
NM_004360.5:c.2439+80T= MANE Select	NP_004351.1:n.2439+80T=
NM_001317184.2:c.2256+80T=	NP_001304113.1:n.2256+80T=
NM_001317185.2:c.891+80T=	NP_001304114.1:n.891+80T=
NM_001317186.2:c.474+80T=	NP_001304115.1:n.474+80T=