Canonical Allele Identifier: CA2229992108

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829681G= , CM000678.2:g.68829681G=	GRCh38
NC_000016.9:g.68863584G= , CM000678.1:g.68863584G=	GRCh37
NC_000016.8:g.67421085G=	NCBI36
NG_008021.1:g.97390G= , LRG_301:g.97390G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2323G= MANE Select	ENSP00000261769.4:p.Gly775=
ENST00000261769.9:c.2323G=	ENSP00000261769.4:p.Gly775=
ENST00000422392.6:c.2140G=	ENSP00000414946.2:p.Gly714=
ENST00000562118.1:n.541G=
ENST00000562836.5:n.2394G=
ENST00000566510.5:c.*989G=	ENSP00000458139.1:n.*989G=
ENST00000566612.5:c.*563G=	ENSP00000454782.1:n.*563G=
ENST00000611625.4:c.2386G=	ENSP00000481063.1:p.Gly796=
ENST00000612417.4:c.1853+3127G=	ENSP00000478360.1:n.1853+3127G=
ENST00000621016.4:c.1866-4522G=	ENSP00000480664.1:n.1866-4522G=
NM_004360.3:c.2323G= , LRG_301t1:c.2323G=	NP_004351.1:p.Gly775=
XM_011523488.1:c.1588G=	XP_011521790.1:p.Gly530=
XM_011523489.1:c.1588G=	XP_011521791.1:p.Gly530=
NM_001317184.1:c.2140G=	NP_001304113.1:p.Gly714=
NM_001317185.1:c.775G=	NP_001304114.1:p.Gly259=
NM_001317186.1:c.358G=	NP_001304115.1:p.Gly120=
NM_004360.4:c.2323G=	NP_004351.1:p.Gly775=
NM_004360.5:c.2323G= MANE Select	NP_004351.1:p.Gly775=
NM_001317184.2:c.2140G=	NP_001304113.1:p.Gly714=
NM_001317185.2:c.775G=	NP_001304114.1:p.Gly259=
NM_001317186.2:c.358G=	NP_001304115.1:p.Gly120=