Canonical Allele Identifier: CA2229980884

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822181C= , CM000678.2:g.68822181C=	GRCh38
NC_000016.9:g.68856084C= , CM000678.1:g.68856084C=	GRCh37
NC_000016.8:g.67413585C=	NCBI36
NG_008021.1:g.89890C= , LRG_301:g.89890C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1892C= MANE Select	ENSP00000261769.4:p.Thr631=
ENST00000261769.9:c.1892C=	ENSP00000261769.4:p.Thr631=
ENST00000422392.6:c.1709C=	ENSP00000414946.2:p.Thr570=
ENST00000562836.5:n.1963C=
ENST00000566510.5:c.*558C=	ENSP00000458139.1:n.*558C=
ENST00000566612.5:c.*132C=	ENSP00000454782.1:n.*132C=
ENST00000611625.4:c.1955C=	ENSP00000481063.1:p.Thr652=
ENST00000612417.4:c.1830+62C=	ENSP00000478360.1:n.1830+62C=
ENST00000621016.4:c.1865+27C=	ENSP00000480664.1:n.1865+27C=
NM_004360.3:c.1892C= , LRG_301t1:c.1892C=	NP_004351.1:p.Thr631=
XM_011523488.1:c.1157C=	XP_011521790.1:p.Thr386=
XM_011523489.1:c.1157C=	XP_011521791.1:p.Thr386=
NM_001317184.1:c.1709C=	NP_001304113.1:p.Thr570=
NM_001317185.1:c.344C=	NP_001304114.1:p.Thr115=
NM_001317186.1:c.-74C=	NP_001304115.1:n.-74C=
NM_004360.4:c.1892C=	NP_004351.1:p.Thr631=
NM_004360.5:c.1892C= MANE Select	NP_004351.1:p.Thr631=
NM_001317184.2:c.1709C=	NP_001304113.1:p.Thr570=
NM_001317185.2:c.344C=	NP_001304114.1:p.Thr115=
NM_001317186.2:c.-74C=	NP_001304115.1:n.-74C=