Canonical Allele Identifier: CA2229975226

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829786T= , CM000678.2:g.68829786T=	GRCh38
NC_000016.9:g.68863689T= , CM000678.1:g.68863689T=	GRCh37
NC_000016.8:g.67421190T=	NCBI36
NG_008021.1:g.97495T= , LRG_301:g.97495T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2428T= MANE Select	ENSP00000261769.4:p.Phe810=
ENST00000261769.9:c.2428T=	ENSP00000261769.4:p.Phe810=
ENST00000422392.6:c.2245T=	ENSP00000414946.2:p.Phe749=
ENST00000562118.1:n.646T=
ENST00000562836.5:n.2499T=
ENST00000566510.5:c.*1094T=	ENSP00000458139.1:n.*1094T=
ENST00000566612.5:c.*668T=	ENSP00000454782.1:n.*668T=
ENST00000611625.4:c.2491T=	ENSP00000481063.1:p.Phe831=
ENST00000612417.4:c.1853+3232T=	ENSP00000478360.1:n.1853+3232T=
ENST00000621016.4:c.1866-4417T=	ENSP00000480664.1:n.1866-4417T=
NM_004360.3:c.2428T= , LRG_301t1:c.2428T=	NP_004351.1:p.Phe810=
XM_011523488.1:c.1693T=	XP_011521790.1:p.Phe565=
XM_011523489.1:c.1693T=	XP_011521791.1:p.Phe565=
NM_001317184.1:c.2245T=	NP_001304113.1:p.Phe749=
NM_001317185.1:c.880T=	NP_001304114.1:p.Phe294=
NM_001317186.1:c.463T=	NP_001304115.1:p.Phe155=
NM_004360.4:c.2428T=	NP_004351.1:p.Phe810=
NM_004360.5:c.2428T= MANE Select	NP_004351.1:p.Phe810=
NM_001317184.2:c.2245T=	NP_001304113.1:p.Phe749=
NM_001317185.2:c.880T=	NP_001304114.1:p.Phe294=
NM_001317186.2:c.463T=	NP_001304115.1:p.Phe155=