Canonical Allele Identifier: CA2229982835

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823461C= , CM000678.2:g.68823461C=	GRCh38
NC_000016.9:g.68857364C= , CM000678.1:g.68857364C=	GRCh37
NC_000016.8:g.67414865C=	NCBI36
NG_008021.1:g.91170C= , LRG_301:g.91170C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1999C= MANE Select	ENSP00000261769.4:p.Leu667=
ENST00000261769.9:c.1999C=	ENSP00000261769.4:p.Leu667=
ENST00000422392.6:c.1816C=	ENSP00000414946.2:p.Leu606=
ENST00000562118.1:n.217C=
ENST00000562836.5:n.2070C=
ENST00000566510.5:c.*665C=	ENSP00000458139.1:n.*665C=
ENST00000566612.5:c.*239C=	ENSP00000454782.1:n.*239C=
ENST00000611625.4:c.2062C=	ENSP00000481063.1:p.Leu688=
ENST00000612417.4:c.1830+1342C=	ENSP00000478360.1:n.1830+1342C=
ENST00000621016.4:c.1865+1307C=	ENSP00000480664.1:n.1865+1307C=
NM_004360.3:c.1999C= , LRG_301t1:c.1999C=	NP_004351.1:p.Leu667=
XM_011523488.1:c.1264C=	XP_011521790.1:p.Leu422=
XM_011523489.1:c.1264C=	XP_011521791.1:p.Leu422=
NM_001317184.1:c.1816C=	NP_001304113.1:p.Leu606=
NM_001317185.1:c.451C=	NP_001304114.1:p.Leu151=
NM_001317186.1:c.34C=	NP_001304115.1:p.Leu12=
NM_004360.4:c.1999C=	NP_004351.1:p.Leu667=
NM_004360.5:c.1999C= MANE Select	NP_004351.1:p.Leu667=
NM_001317184.2:c.1816C=	NP_001304113.1:p.Leu606=
NM_001317185.2:c.451C=	NP_001304114.1:p.Leu151=
NM_001317186.2:c.34C=	NP_001304115.1:p.Leu12=