Canonical Allele Identifier: CA2229964958

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68808485G= , CM000678.2:g.68808485G=	GRCh38
NC_000016.9:g.68842388G= , CM000678.1:g.68842388G=	GRCh37
NC_000016.8:g.67399889G=	NCBI36
NG_008021.1:g.76194G= , LRG_301:g.76194G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.449G= MANE Select	ENSP00000261769.4:p.Arg150=
ENST00000261769.9:c.449G=	ENSP00000261769.4:p.Arg150=
ENST00000422392.6:c.449G=	ENSP00000414946.2:p.Arg150=
ENST00000561751.1:c.216G=
ENST00000562836.5:n.520G=
ENST00000564676.5:n.731G=
ENST00000564745.1:n.444G=
ENST00000566510.5:c.449G=	ENSP00000458139.1:p.Arg150=
ENST00000566612.5:c.449G=	ENSP00000454782.1:p.Arg150=
ENST00000611625.4:c.449G=	ENSP00000481063.1:p.Arg150=
ENST00000612417.4:c.449G=	ENSP00000478360.1:p.Arg150=
ENST00000621016.4:c.449G=	ENSP00000480664.1:p.Arg150=
NM_004360.3:c.449G= , LRG_301t1:c.449G=	NP_004351.1:p.Arg150=
XM_011523488.1:c.-287G=	XP_011521790.1:n.-287G=
XM_011523489.1:c.-287G=	XP_011521791.1:n.-287G=
NM_001317184.1:c.449G=	NP_001304113.1:p.Arg150=
NM_001317185.1:c.-1167G=	NP_001304114.1:n.-1167G=
NM_001317186.1:c.-1371G=	NP_001304115.1:n.-1371G=
NM_004360.4:c.449G=	NP_004351.1:p.Arg150=
NM_004360.5:c.449G= MANE Select	NP_004351.1:p.Arg150=
NM_001317184.2:c.449G=	NP_001304113.1:p.Arg150=
NM_001317185.2:c.-1167G=	NP_001304114.1:n.-1167G=
NM_001317186.2:c.-1371G=	NP_001304115.1:n.-1371G=