Canonical Allele Identifier: CA2229992174

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829690G= , CM000678.2:g.68829690G=	GRCh38
NC_000016.9:g.68863593G= , CM000678.1:g.68863593G=	GRCh37
NC_000016.8:g.67421094G=	NCBI36
NG_008021.1:g.97399G= , LRG_301:g.97399G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2332G= MANE Select	ENSP00000261769.4:p.Ala778=
ENST00000261769.9:c.2332G=	ENSP00000261769.4:p.Ala778=
ENST00000422392.6:c.2149G=	ENSP00000414946.2:p.Ala717=
ENST00000562118.1:n.550G=
ENST00000562836.5:n.2403G=
ENST00000566510.5:c.*998G=	ENSP00000458139.1:n.*998G=
ENST00000566612.5:c.*572G=	ENSP00000454782.1:n.*572G=
ENST00000611625.4:c.2395G=	ENSP00000481063.1:p.Ala799=
ENST00000612417.4:c.1853+3136G=	ENSP00000478360.1:n.1853+3136G=
ENST00000621016.4:c.1866-4513G=	ENSP00000480664.1:n.1866-4513G=
NM_004360.3:c.2332G= , LRG_301t1:c.2332G=	NP_004351.1:p.Ala778=
XM_011523488.1:c.1597G=	XP_011521790.1:p.Ala533=
XM_011523489.1:c.1597G=	XP_011521791.1:p.Ala533=
NM_001317184.1:c.2149G=	NP_001304113.1:p.Ala717=
NM_001317185.1:c.784G=	NP_001304114.1:p.Ala262=
NM_001317186.1:c.367G=	NP_001304115.1:p.Ala123=
NM_004360.4:c.2332G=	NP_004351.1:p.Ala778=
NM_004360.5:c.2332G= MANE Select	NP_004351.1:p.Ala778=
NM_001317184.2:c.2149G=	NP_001304113.1:p.Ala717=
NM_001317185.2:c.784G=	NP_001304114.1:p.Ala262=
NM_001317186.2:c.367G=	NP_001304115.1:p.Ala123=