Canonical Allele Identifier: CA2229980630

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822122C= , CM000678.2:g.68822122C=	GRCh38
NC_000016.9:g.68856025C= , CM000678.1:g.68856025C=	GRCh37
NC_000016.8:g.67413526C=	NCBI36
NG_008021.1:g.89831C= , LRG_301:g.89831C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1833C= MANE Select	ENSP00000261769.4:p.Val611=
ENST00000261769.9:c.1833C=	ENSP00000261769.4:p.Val611=
ENST00000422392.6:c.1650C=	ENSP00000414946.2:p.Val550=
ENST00000562836.5:n.1904C=
ENST00000566510.5:c.*499C=	ENSP00000458139.1:n.*499C=
ENST00000566612.5:c.*73C=	ENSP00000454782.1:n.*73C=
ENST00000611625.4:c.1896C=	ENSP00000481063.1:p.Val632=
ENST00000612417.4:c.1830+3C=	ENSP00000478360.1:n.1830+3C=
ENST00000621016.4:c.1833C=	ENSP00000480664.1:p.Val611=
NM_004360.3:c.1833C= , LRG_301t1:c.1833C=	NP_004351.1:p.Val611=
XM_011523488.1:c.1098C=	XP_011521790.1:p.Val366=
XM_011523489.1:c.1098C=	XP_011521791.1:p.Val366=
NM_001317184.1:c.1650C=	NP_001304113.1:p.Val550=
NM_001317185.1:c.285C=	NP_001304114.1:p.Val95=
NM_001317186.1:c.-133C=	NP_001304115.1:n.-133C=
NM_004360.4:c.1833C=	NP_004351.1:p.Val611=
NM_004360.5:c.1833C= MANE Select	NP_004351.1:p.Val611=
NM_001317184.2:c.1650C=	NP_001304113.1:p.Val550=
NM_001317185.2:c.285C=	NP_001304114.1:p.Val95=
NM_001317186.2:c.-133C=	NP_001304115.1:n.-133C=