Canonical Allele Identifier: CA2229983199

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823547T= , CM000678.2:g.68823547T=	GRCh38
NC_000016.9:g.68857450T= , CM000678.1:g.68857450T=	GRCh37
NC_000016.8:g.67414951T=	NCBI36
NG_008021.1:g.91256T= , LRG_301:g.91256T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2085T= MANE Select	ENSP00000261769.4:p.Cys695=
ENST00000261769.9:c.2085T=	ENSP00000261769.4:p.Cys695=
ENST00000422392.6:c.1902T=	ENSP00000414946.2:p.Cys634=
ENST00000562118.1:n.303T=
ENST00000562836.5:n.2156T=
ENST00000566510.5:c.*751T=	ENSP00000458139.1:n.*751T=
ENST00000566612.5:c.*325T=	ENSP00000454782.1:n.*325T=
ENST00000611625.4:c.2148T=	ENSP00000481063.1:p.Cys716=
ENST00000612417.4:c.1830+1428T=	ENSP00000478360.1:n.1830+1428T=
ENST00000621016.4:c.1865+1393T=	ENSP00000480664.1:n.1865+1393T=
NM_004360.3:c.2085T= , LRG_301t1:c.2085T=	NP_004351.1:p.Cys695=
XM_011523488.1:c.1350T=	XP_011521790.1:p.Cys450=
XM_011523489.1:c.1350T=	XP_011521791.1:p.Cys450=
NM_001317184.1:c.1902T=	NP_001304113.1:p.Cys634=
NM_001317185.1:c.537T=	NP_001304114.1:p.Cys179=
NM_001317186.1:c.120T=	NP_001304115.1:p.Cys40=
NM_004360.4:c.2085T=	NP_004351.1:p.Cys695=
NM_004360.5:c.2085T= MANE Select	NP_004351.1:p.Cys695=
NM_001317184.2:c.1902T=	NP_001304113.1:p.Cys634=
NM_001317185.2:c.537T=	NP_001304114.1:p.Cys179=
NM_001317186.2:c.120T=	NP_001304115.1:p.Cys40=