Canonical Allele Identifier: CA2229958006

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68801838C= , CM000678.2:g.68801838C=	GRCh38
NC_000016.9:g.68835741C= , CM000678.1:g.68835741C=	GRCh37
NC_000016.8:g.67393242C=	NCBI36
NG_008021.1:g.69547C= , LRG_301:g.69547C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.332C= MANE Select	ENSP00000261769.4:p.Ser111=
ENST00000261769.9:c.332C=	ENSP00000261769.4:p.Ser111=
ENST00000422392.6:c.332C=	ENSP00000414946.2:p.Ser111=
ENST00000561751.1:c.99C=
ENST00000562836.5:n.403C=
ENST00000564676.5:n.614C=
ENST00000564745.1:n.327C=
ENST00000566510.5:c.332C=	ENSP00000458139.1:p.Ser111=
ENST00000566612.5:c.332C=	ENSP00000454782.1:p.Ser111=
ENST00000611625.4:c.332C=	ENSP00000481063.1:p.Ser111=
ENST00000612417.4:c.332C=	ENSP00000478360.1:p.Ser111=
ENST00000621016.4:c.332C=	ENSP00000480664.1:p.Ser111=
NM_004360.3:c.332C= , LRG_301t1:c.332C=	NP_004351.1:p.Ser111=
XM_011523488.1:c.-404C=	XP_011521790.1:n.-404C=
XM_011523489.1:c.-404C=	XP_011521791.1:n.-404C=
NM_001317184.1:c.332C=	NP_001304113.1:p.Ser111=
NM_001317185.1:c.-1284C=	NP_001304114.1:n.-1284C=
NM_001317186.1:c.-1488C=	NP_001304115.1:n.-1488C=
NM_004360.4:c.332C=	NP_004351.1:p.Ser111=
NM_004360.5:c.332C= MANE Select	NP_004351.1:p.Ser111=
NM_001317184.2:c.332C=	NP_001304113.1:p.Ser111=
NM_001317185.2:c.-1284C=	NP_001304114.1:n.-1284C=
NM_001317186.2:c.-1488C=	NP_001304115.1:n.-1488C=