Canonical Allele Identifier: CA2229957850

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68801799T= , CM000678.2:g.68801799T=	GRCh38
NC_000016.9:g.68835702T= , CM000678.1:g.68835702T=	GRCh37
NC_000016.8:g.67393203T=	NCBI36
NG_008021.1:g.69508T= , LRG_301:g.69508T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.293T= MANE Select	ENSP00000261769.4:p.Phe98=
ENST00000261769.9:c.293T=	ENSP00000261769.4:p.Phe98=
ENST00000422392.6:c.293T=	ENSP00000414946.2:p.Phe98=
ENST00000561751.1:c.60T=
ENST00000562836.5:n.364T=
ENST00000564676.5:n.575T=
ENST00000564745.1:n.288T=
ENST00000566510.5:c.293T=	ENSP00000458139.1:p.Phe98=
ENST00000566612.5:c.293T=	ENSP00000454782.1:p.Phe98=
ENST00000611625.4:c.293T=	ENSP00000481063.1:p.Phe98=
ENST00000612417.4:c.293T=	ENSP00000478360.1:p.Phe98=
ENST00000621016.4:c.293T=	ENSP00000480664.1:p.Phe98=
NM_004360.3:c.293T= , LRG_301t1:c.293T=	NP_004351.1:p.Phe98=
XM_011523488.1:c.-443T=	XP_011521790.1:n.-443T=
XM_011523489.1:c.-443T=	XP_011521791.1:n.-443T=
NM_001317184.1:c.293T=	NP_001304113.1:p.Phe98=
NM_001317185.1:c.-1323T=	NP_001304114.1:n.-1323T=
NM_001317186.1:c.-1527T=	NP_001304115.1:n.-1527T=
NM_004360.4:c.293T=	NP_004351.1:p.Phe98=
NM_004360.5:c.293T= MANE Select	NP_004351.1:p.Phe98=
NM_001317184.2:c.293T=	NP_001304113.1:p.Phe98=
NM_001317185.2:c.-1323T=	NP_001304114.1:n.-1323T=
NM_001317186.2:c.-1527T=	NP_001304115.1:n.-1527T=