Canonical Allele Identifier: CA2229978186

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833364C= , CM000678.2:g.68833364C=	GRCh38
NC_000016.9:g.68867267C= , CM000678.1:g.68867267C=	GRCh37
NC_000016.8:g.67424768C=	NCBI36
NG_008021.1:g.101073C= , LRG_301:g.101073C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2514C= MANE Select	ENSP00000261769.4:p.Ser838=
ENST00000261769.9:c.2514C=	ENSP00000261769.4:p.Ser838=
ENST00000422392.6:c.2331C=	ENSP00000414946.2:p.Ser777=
ENST00000562118.1:n.732C=
ENST00000562836.5:n.2585C=
ENST00000566510.5:c.*1180C=	ENSP00000458139.1:n.*1180C=
ENST00000566612.5:c.*754C=	ENSP00000454782.1:n.*754C=
ENST00000611625.4:c.2577C=	ENSP00000481063.1:p.Ser859=
ENST00000612417.4:c.1854-827C=	ENSP00000478360.1:n.1854-827C=
ENST00000621016.4:c.1866-839C=	ENSP00000480664.1:n.1866-839C=
NM_004360.3:c.2514C= , LRG_301t1:c.2514C=	NP_004351.1:p.Ser838=
XM_011523488.1:c.1779C=	XP_011521790.1:p.Ser593=
XM_011523489.1:c.1779C=	XP_011521791.1:p.Ser593=
NM_001317184.1:c.2331C=	NP_001304113.1:p.Ser777=
NM_001317185.1:c.966C=	NP_001304114.1:p.Ser322=
NM_001317186.1:c.549C=	NP_001304115.1:p.Ser183=
NM_004360.4:c.2514C=	NP_004351.1:p.Ser838=
NM_004360.5:c.2514C= MANE Select	NP_004351.1:p.Ser838=
NM_001317184.2:c.2331C=	NP_001304113.1:p.Ser777=
NM_001317185.2:c.966C=	NP_001304114.1:p.Ser322=
NM_001317186.2:c.549C=	NP_001304115.1:p.Ser183=