Canonical Allele Identifier: CA2229992009

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829660G= , CM000678.2:g.68829660G=	GRCh38
NC_000016.9:g.68863563G= , CM000678.1:g.68863563G=	GRCh37
NC_000016.8:g.67421064G=	NCBI36
NG_008021.1:g.97369G= , LRG_301:g.97369G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2302G= MANE Select	ENSP00000261769.4:p.Asp768=
ENST00000261769.9:c.2302G=	ENSP00000261769.4:p.Asp768=
ENST00000422392.6:c.2119G=	ENSP00000414946.2:p.Asp707=
ENST00000562118.1:n.520G=
ENST00000562836.5:n.2373G=
ENST00000566510.5:c.*968G=	ENSP00000458139.1:n.*968G=
ENST00000566612.5:c.*542G=	ENSP00000454782.1:n.*542G=
ENST00000611625.4:c.2365G=	ENSP00000481063.1:p.Asp789=
ENST00000612417.4:c.1853+3106G=	ENSP00000478360.1:n.1853+3106G=
ENST00000621016.4:c.1866-4543G=	ENSP00000480664.1:n.1866-4543G=
NM_004360.3:c.2302G= , LRG_301t1:c.2302G=	NP_004351.1:p.Asp768=
XM_011523488.1:c.1567G=	XP_011521790.1:p.Asp523=
XM_011523489.1:c.1567G=	XP_011521791.1:p.Asp523=
NM_001317184.1:c.2119G=	NP_001304113.1:p.Asp707=
NM_001317185.1:c.754G=	NP_001304114.1:p.Asp252=
NM_001317186.1:c.337G=	NP_001304115.1:p.Asp113=
NM_004360.4:c.2302G=	NP_004351.1:p.Asp768=
NM_004360.5:c.2302G= MANE Select	NP_004351.1:p.Asp768=
NM_001317184.2:c.2119G=	NP_001304113.1:p.Asp707=
NM_001317185.2:c.754G=	NP_001304114.1:p.Asp252=
NM_001317186.2:c.337G=	NP_001304115.1:p.Asp113=