Canonical Allele Identifier: CA2229977914

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68819309G= , CM000678.2:g.68819309G=	GRCh38
NC_000016.9:g.68853212G= , CM000678.1:g.68853212G=	GRCh37
NC_000016.8:g.67410713G=	NCBI36
NG_008021.1:g.87018G= , LRG_301:g.87018G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1595G= MANE Select	ENSP00000261769.4:p.Trp532=
ENST00000261769.9:c.1595G=	ENSP00000261769.4:p.Trp532=
ENST00000422392.6:c.1412G=	ENSP00000414946.2:p.Trp471=
ENST00000562836.5:n.1666G=
ENST00000566510.5:c.*261G=	ENSP00000458139.1:n.*261G=
ENST00000566612.5:c.1566-2692G=	ENSP00000454782.1:n.1566-2692G=
ENST00000611625.4:c.1658G=	ENSP00000481063.1:p.Trp553=
ENST00000612417.4:c.1595G=	ENSP00000478360.1:p.Trp532=
ENST00000621016.4:c.1595G=	ENSP00000480664.1:p.Trp532=
NM_004360.3:c.1595G= , LRG_301t1:c.1595G=	NP_004351.1:p.Trp532=
XM_011523488.1:c.860G=	XP_011521790.1:p.Trp287=
XM_011523489.1:c.860G=	XP_011521791.1:p.Trp287=
NM_001317184.1:c.1412G=	NP_001304113.1:p.Trp471=
NM_001317185.1:c.47G=	NP_001304114.1:p.Trp16=
NM_001317186.1:c.-254-2692G=	NP_001304115.1:n.-254-2692G=
NM_004360.4:c.1595G=	NP_004351.1:p.Trp532=
NM_004360.5:c.1595G= MANE Select	NP_004351.1:p.Trp532=
NM_001317184.2:c.1412G=	NP_001304113.1:p.Trp471=
NM_001317185.2:c.47G=	NP_001304114.1:p.Trp16=
NM_001317186.2:c.-254-2692G=	NP_001304115.1:n.-254-2692G=