Canonical Allele Identifier: CA2229980541

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822085C= , CM000678.2:g.68822085C=	GRCh38
NC_000016.9:g.68855988C= , CM000678.1:g.68855988C=	GRCh37
NC_000016.8:g.67413489C=	NCBI36
NG_008021.1:g.89794C= , LRG_301:g.89794C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1796C= MANE Select	ENSP00000261769.4:p.Thr599=
ENST00000261769.9:c.1796C=	ENSP00000261769.4:p.Thr599=
ENST00000422392.6:c.1613C=	ENSP00000414946.2:p.Thr538=
ENST00000562836.5:n.1867C=
ENST00000566510.5:c.*462C=	ENSP00000458139.1:n.*462C=
ENST00000566612.5:c.*36C=	ENSP00000454782.1:n.*36C=
ENST00000611625.4:c.1859C=	ENSP00000481063.1:p.Thr620=
ENST00000612417.4:c.1796C=	ENSP00000478360.1:p.Thr599=
ENST00000621016.4:c.1796C=	ENSP00000480664.1:p.Thr599=
NM_004360.3:c.1796C= , LRG_301t1:c.1796C=	NP_004351.1:p.Thr599=
XM_011523488.1:c.1061C=	XP_011521790.1:p.Thr354=
XM_011523489.1:c.1061C=	XP_011521791.1:p.Thr354=
NM_001317184.1:c.1613C=	NP_001304113.1:p.Thr538=
NM_001317185.1:c.248C=	NP_001304114.1:p.Thr83=
NM_001317186.1:c.-170C=	NP_001304115.1:n.-170C=
NM_004360.4:c.1796C=	NP_004351.1:p.Thr599=
NM_004360.5:c.1796C= MANE Select	NP_004351.1:p.Thr599=
NM_001317184.2:c.1613C=	NP_001304113.1:p.Thr538=
NM_001317185.2:c.248C=	NP_001304114.1:p.Thr83=
NM_001317186.2:c.-170C=	NP_001304115.1:n.-170C=