Canonical Allele Identifier: CA2229981983

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823108G= , CM000678.2:g.68823108G=	GRCh38
NC_000016.9:g.68857011G= , CM000678.1:g.68857011G=	GRCh37
NC_000016.8:g.67414512G=	NCBI36
NG_008021.1:g.90817G= , LRG_301:g.90817G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1937-291G= MANE Select	ENSP00000261769.4:n.1937-291G=
ENST00000261769.9:c.1937-291G=	ENSP00000261769.4:n.1937-291G=
ENST00000422392.6:c.1754-291G=	ENSP00000414946.2:n.1754-291G=
ENST00000562836.5:n.2008-291G=
ENST00000566510.5:c.*603-291G=	ENSP00000458139.1:n.*603-291G=
ENST00000566612.5:c.*177-291G=	ENSP00000454782.1:n.*177-291G=
ENST00000611625.4:c.2000-291G=	ENSP00000481063.1:n.2000-291G=
ENST00000612417.4:c.1830+989G=	ENSP00000478360.1:n.1830+989G=
ENST00000621016.4:c.1865+954G=	ENSP00000480664.1:n.1865+954G=
NM_004360.3:c.1937-291G= , LRG_301t1:c.1937-291G=	NP_004351.1:n.1937-291G=
XM_011523488.1:c.1202-291G=	XP_011521790.1:n.1202-291G=
XM_011523489.1:c.1202-291G=	XP_011521791.1:n.1202-291G=
NM_001317184.1:c.1754-291G=	NP_001304113.1:n.1754-291G=
NM_001317185.1:c.389-291G=	NP_001304114.1:n.389-291G=
NM_001317186.1:c.-29-291G=	NP_001304115.1:n.-29-291G=
NM_004360.4:c.1937-291G=	NP_004351.1:n.1937-291G=
NM_004360.5:c.1937-291G= MANE Select	NP_004351.1:n.1937-291G=
NM_001317184.2:c.1754-291G=	NP_001304113.1:n.1754-291G=
NM_001317185.2:c.389-291G=	NP_001304114.1:n.389-291G=
NM_001317186.2:c.-29-291G=	NP_001304115.1:n.-29-291G=