Canonical Allele Identifier: CA2229916472

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68738316A= , CM000678.2:g.68738316A=	GRCh38
NC_000016.9:g.68772219A= , CM000678.1:g.68772219A=	GRCh37
NC_000016.8:g.67329720A=	NCBI36
NG_008021.1:g.6025A= , LRG_301:g.6025A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.68A= MANE Select	ENSP00000261769.4:p.Gln23=
ENST00000261769.9:c.68A=	ENSP00000261769.4:p.Gln23=
ENST00000422392.6:c.68A=	ENSP00000414946.2:p.Gln23=
ENST00000566510.5:c.68A=	ENSP00000458139.1:p.Gln23=
ENST00000566612.5:c.68A=	ENSP00000454782.1:p.Gln23=
ENST00000611625.4:c.68A=	ENSP00000481063.1:p.Gln23=
ENST00000612417.4:c.68A=	ENSP00000478360.1:p.Gln23=
ENST00000621016.4:c.68A=	ENSP00000480664.1:p.Gln23=
NM_004360.3:c.68A= , LRG_301t1:c.68A=	NP_004351.1:p.Gln23=
NM_001317184.1:c.68A=	NP_001304113.1:p.Gln23=
NM_001317185.1:c.-1548A=	NP_001304114.1:n.-1548A=
NM_001317186.1:c.-1752A=	NP_001304115.1:n.-1752A=
NM_004360.4:c.68A=	NP_004351.1:p.Gln23=
NM_004360.5:c.68A= MANE Select	NP_004351.1:p.Gln23=
NM_001317184.2:c.68A=	NP_001304113.1:p.Gln23=
NM_001317185.2:c.-1548A=	NP_001304114.1:n.-1548A=
NM_001317186.2:c.-1752A=	NP_001304115.1:n.-1752A=