Canonical Allele Identifier: CA2229978255

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833393T= , CM000678.2:g.68833393T=	GRCh38
NC_000016.9:g.68867296T= , CM000678.1:g.68867296T=	GRCh37
NC_000016.8:g.67424797T=	NCBI36
NG_008021.1:g.101102T= , LRG_301:g.101102T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2543T= MANE Select	ENSP00000261769.4:p.Leu848=
ENST00000261769.9:c.2543T=	ENSP00000261769.4:p.Leu848=
ENST00000422392.6:c.2360T=	ENSP00000414946.2:p.Leu787=
ENST00000562118.1:n.761T=
ENST00000562836.5:n.2614T=
ENST00000566510.5:c.*1209T=	ENSP00000458139.1:n.*1209T=
ENST00000566612.5:c.*783T=	ENSP00000454782.1:n.*783T=
ENST00000611625.4:c.2606T=	ENSP00000481063.1:p.Leu869=
ENST00000612417.4:c.1854-798T=	ENSP00000478360.1:n.1854-798T=
ENST00000621016.4:c.1866-810T=	ENSP00000480664.1:n.1866-810T=
NM_004360.3:c.2543T= , LRG_301t1:c.2543T=	NP_004351.1:p.Leu848=
XM_011523488.1:c.1808T=	XP_011521790.1:p.Leu603=
XM_011523489.1:c.1808T=	XP_011521791.1:p.Leu603=
NM_001317184.1:c.2360T=	NP_001304113.1:p.Leu787=
NM_001317185.1:c.995T=	NP_001304114.1:p.Leu332=
NM_001317186.1:c.578T=	NP_001304115.1:p.Leu193=
NM_004360.4:c.2543T=	NP_004351.1:p.Leu848=
NM_004360.5:c.2543T= MANE Select	NP_004351.1:p.Leu848=
NM_001317184.2:c.2360T=	NP_001304113.1:p.Leu787=
NM_001317185.2:c.995T=	NP_001304114.1:p.Leu332=
NM_001317186.2:c.578T=	NP_001304115.1:p.Leu193=