Canonical Allele Identifier: CA2229978471

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833447G= , CM000678.2:g.68833447G=	GRCh38
NC_000016.9:g.68867350G= , CM000678.1:g.68867350G=	GRCh37
NC_000016.8:g.67424851G=	NCBI36
NG_008021.1:g.101156G= , LRG_301:g.101156G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2597G= MANE Select	ENSP00000261769.4:p.Gly866=
ENST00000261769.9:c.2597G=	ENSP00000261769.4:p.Gly866=
ENST00000422392.6:c.2414G=	ENSP00000414946.2:p.Gly805=
ENST00000562118.1:n.815G=
ENST00000562836.5:n.2668G=
ENST00000566510.5:c.*1263G=	ENSP00000458139.1:n.*1263G=
ENST00000566612.5:c.*837G=	ENSP00000454782.1:n.*837G=
ENST00000611625.4:c.2660G=	ENSP00000481063.1:p.Gly887=
ENST00000612417.4:c.1854-744G=	ENSP00000478360.1:n.1854-744G=
ENST00000621016.4:c.1866-756G=	ENSP00000480664.1:n.1866-756G=
NM_004360.3:c.2597G= , LRG_301t1:c.2597G=	NP_004351.1:p.Gly866=
XM_011523488.1:c.1862G=	XP_011521790.1:p.Gly621=
XM_011523489.1:c.1862G=	XP_011521791.1:p.Gly621=
NM_001317184.1:c.2414G=	NP_001304113.1:p.Gly805=
NM_001317185.1:c.1049G=	NP_001304114.1:p.Gly350=
NM_001317186.1:c.632G=	NP_001304115.1:p.Gly211=
NM_004360.4:c.2597G=	NP_004351.1:p.Gly866=
NM_004360.5:c.2597G= MANE Select	NP_004351.1:p.Gly866=
NM_001317184.2:c.2414G=	NP_001304113.1:p.Gly805=
NM_001317185.2:c.1049G=	NP_001304114.1:p.Gly350=
NM_001317186.2:c.632G=	NP_001304115.1:p.Gly211=