Canonical Allele Identifier: CA2229980919

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822186G= , CM000678.2:g.68822186G=	GRCh38
NC_000016.9:g.68856089G= , CM000678.1:g.68856089G=	GRCh37
NC_000016.8:g.67413590G=	NCBI36
NG_008021.1:g.89895G= , LRG_301:g.89895G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1897G= MANE Select	ENSP00000261769.4:p.Gly633=
ENST00000261769.9:c.1897G=	ENSP00000261769.4:p.Gly633=
ENST00000422392.6:c.1714G=	ENSP00000414946.2:p.Gly572=
ENST00000562836.5:n.1968G=
ENST00000566510.5:c.*563G=	ENSP00000458139.1:n.*563G=
ENST00000566612.5:c.*137G=	ENSP00000454782.1:n.*137G=
ENST00000611625.4:c.1960G=	ENSP00000481063.1:p.Gly654=
ENST00000612417.4:c.1830+67G=	ENSP00000478360.1:n.1830+67G=
ENST00000621016.4:c.1865+32G=	ENSP00000480664.1:n.1865+32G=
NM_004360.3:c.1897G= , LRG_301t1:c.1897G=	NP_004351.1:p.Gly633=
XM_011523488.1:c.1162G=	XP_011521790.1:p.Gly388=
XM_011523489.1:c.1162G=	XP_011521791.1:p.Gly388=
NM_001317184.1:c.1714G=	NP_001304113.1:p.Gly572=
NM_001317185.1:c.349G=	NP_001304114.1:p.Gly117=
NM_001317186.1:c.-69G=	NP_001304115.1:n.-69G=
NM_004360.4:c.1897G=	NP_004351.1:p.Gly633=
NM_004360.5:c.1897G= MANE Select	NP_004351.1:p.Gly633=
NM_001317184.2:c.1714G=	NP_001304113.1:p.Gly572=
NM_001317185.2:c.349G=	NP_001304114.1:p.Gly117=
NM_001317186.2:c.-69G=	NP_001304115.1:n.-69G=