Canonical Allele Identifier: CA2229980984

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822199A= , CM000678.2:g.68822199A=	GRCh38
NC_000016.9:g.68856102A= , CM000678.1:g.68856102A=	GRCh37
NC_000016.8:g.67413603A=	NCBI36
NG_008021.1:g.89908A= , LRG_301:g.89908A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1910A= MANE Select	ENSP00000261769.4:p.Asn637=
ENST00000261769.9:c.1910A=	ENSP00000261769.4:p.Asn637=
ENST00000422392.6:c.1727A=	ENSP00000414946.2:p.Asn576=
ENST00000562836.5:n.1981A=
ENST00000566510.5:c.*576A=	ENSP00000458139.1:n.*576A=
ENST00000566612.5:c.*150A=	ENSP00000454782.1:n.*150A=
ENST00000611625.4:c.1973A=	ENSP00000481063.1:p.Asn658=
ENST00000612417.4:c.1830+80A=	ENSP00000478360.1:n.1830+80A=
ENST00000621016.4:c.1865+45A=	ENSP00000480664.1:n.1865+45A=
NM_004360.3:c.1910A= , LRG_301t1:c.1910A=	NP_004351.1:p.Asn637=
XM_011523488.1:c.1175A=	XP_011521790.1:p.Asn392=
XM_011523489.1:c.1175A=	XP_011521791.1:p.Asn392=
NM_001317184.1:c.1727A=	NP_001304113.1:p.Asn576=
NM_001317185.1:c.362A=	NP_001304114.1:p.Asn121=
NM_001317186.1:c.-56A=	NP_001304115.1:n.-56A=
NM_004360.4:c.1910A=	NP_004351.1:p.Asn637=
NM_004360.5:c.1910A= MANE Select	NP_004351.1:p.Asn637=
NM_001317184.2:c.1727A=	NP_001304113.1:p.Asn576=
NM_001317185.2:c.362A=	NP_001304114.1:p.Asn121=
NM_001317186.2:c.-56A=	NP_001304115.1:n.-56A=