Canonical Allele Identifier: CA2229983168

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823538T= , CM000678.2:g.68823538T=	GRCh38
NC_000016.9:g.68857441T= , CM000678.1:g.68857441T=	GRCh37
NC_000016.8:g.67414942T=	NCBI36
NG_008021.1:g.91247T= , LRG_301:g.91247T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2076T= MANE Select	ENSP00000261769.4:p.Ala692=
ENST00000261769.9:c.2076T=	ENSP00000261769.4:p.Ala692=
ENST00000422392.6:c.1893T=	ENSP00000414946.2:p.Ala631=
ENST00000562118.1:n.294T=
ENST00000562836.5:n.2147T=
ENST00000566510.5:c.*742T=	ENSP00000458139.1:n.*742T=
ENST00000566612.5:c.*316T=	ENSP00000454782.1:n.*316T=
ENST00000611625.4:c.2139T=	ENSP00000481063.1:p.Ala713=
ENST00000612417.4:c.1830+1419T=	ENSP00000478360.1:n.1830+1419T=
ENST00000621016.4:c.1865+1384T=	ENSP00000480664.1:n.1865+1384T=
NM_004360.3:c.2076T= , LRG_301t1:c.2076T=	NP_004351.1:p.Ala692=
XM_011523488.1:c.1341T=	XP_011521790.1:p.Ala447=
XM_011523489.1:c.1341T=	XP_011521791.1:p.Ala447=
NM_001317184.1:c.1893T=	NP_001304113.1:p.Ala631=
NM_001317185.1:c.528T=	NP_001304114.1:p.Ala176=
NM_001317186.1:c.111T=	NP_001304115.1:p.Ala37=
NM_004360.4:c.2076T=	NP_004351.1:p.Ala692=
NM_004360.5:c.2076T= MANE Select	NP_004351.1:p.Ala692=
NM_001317184.2:c.1893T=	NP_001304113.1:p.Ala631=
NM_001317185.2:c.528T=	NP_001304114.1:p.Ala176=
NM_001317186.2:c.111T=	NP_001304115.1:p.Ala37=