Canonical Allele Identifier: CA2229980679

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822133T= , CM000678.2:g.68822133T=	GRCh38
NC_000016.9:g.68856036T= , CM000678.1:g.68856036T=	GRCh37
NC_000016.8:g.67413537T=	NCBI36
NG_008021.1:g.89842T= , LRG_301:g.89842T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1844T= MANE Select	ENSP00000261769.4:p.Ile615=
ENST00000261769.9:c.1844T=	ENSP00000261769.4:p.Ile615=
ENST00000422392.6:c.1661T=	ENSP00000414946.2:p.Ile554=
ENST00000562836.5:n.1915T=
ENST00000566510.5:c.*510T=	ENSP00000458139.1:n.*510T=
ENST00000566612.5:c.*84T=	ENSP00000454782.1:n.*84T=
ENST00000611625.4:c.1907T=	ENSP00000481063.1:p.Ile636=
ENST00000612417.4:c.1830+14T=	ENSP00000478360.1:n.1830+14T=
ENST00000621016.4:c.1844T=	ENSP00000480664.1:p.Ile615=
NM_004360.3:c.1844T= , LRG_301t1:c.1844T=	NP_004351.1:p.Ile615=
XM_011523488.1:c.1109T=	XP_011521790.1:p.Ile370=
XM_011523489.1:c.1109T=	XP_011521791.1:p.Ile370=
NM_001317184.1:c.1661T=	NP_001304113.1:p.Ile554=
NM_001317185.1:c.296T=	NP_001304114.1:p.Ile99=
NM_001317186.1:c.-122T=	NP_001304115.1:n.-122T=
NM_004360.4:c.1844T=	NP_004351.1:p.Ile615=
NM_004360.5:c.1844T= MANE Select	NP_004351.1:p.Ile615=
NM_001317184.2:c.1661T=	NP_001304113.1:p.Ile554=
NM_001317185.2:c.296T=	NP_001304114.1:p.Ile99=
NM_001317186.2:c.-122T=	NP_001304115.1:n.-122T=