Canonical Allele Identifier: CA2229981035

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822211A= , CM000678.2:g.68822211A=	GRCh38
NC_000016.9:g.68856114A= , CM000678.1:g.68856114A=	GRCh37
NC_000016.8:g.67413615A=	NCBI36
NG_008021.1:g.89920A= , LRG_301:g.89920A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1922A= MANE Select	ENSP00000261769.4:p.Gln641=
ENST00000261769.9:c.1922A=	ENSP00000261769.4:p.Gln641=
ENST00000422392.6:c.1739A=	ENSP00000414946.2:p.Gln580=
ENST00000562836.5:n.1993A=
ENST00000566510.5:c.*588A=	ENSP00000458139.1:n.*588A=
ENST00000566612.5:c.*162A=	ENSP00000454782.1:n.*162A=
ENST00000611625.4:c.1985A=	ENSP00000481063.1:p.Gln662=
ENST00000612417.4:c.1830+92A=	ENSP00000478360.1:n.1830+92A=
ENST00000621016.4:c.1865+57A=	ENSP00000480664.1:n.1865+57A=
NM_004360.3:c.1922A= , LRG_301t1:c.1922A=	NP_004351.1:p.Gln641=
XM_011523488.1:c.1187A=	XP_011521790.1:p.Gln396=
XM_011523489.1:c.1187A=	XP_011521791.1:p.Gln396=
NM_001317184.1:c.1739A=	NP_001304113.1:p.Gln580=
NM_001317185.1:c.374A=	NP_001304114.1:p.Gln125=
NM_001317186.1:c.-44A=	NP_001304115.1:n.-44A=
NM_004360.4:c.1922A=	NP_004351.1:p.Gln641=
NM_004360.5:c.1922A= MANE Select	NP_004351.1:p.Gln641=
NM_001317184.2:c.1739A=	NP_001304113.1:p.Gln580=
NM_001317185.2:c.374A=	NP_001304114.1:p.Gln125=
NM_001317186.2:c.-44A=	NP_001304115.1:n.-44A=