Canonical Allele Identifier: CA2229980938

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822189G= , CM000678.2:g.68822189G=	GRCh38
NC_000016.9:g.68856092G= , CM000678.1:g.68856092G=	GRCh37
NC_000016.8:g.67413593G=	NCBI36
NG_008021.1:g.89898G= , LRG_301:g.89898G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1900G= MANE Select	ENSP00000261769.4:p.Ala634=
ENST00000261769.9:c.1900G=	ENSP00000261769.4:p.Ala634=
ENST00000422392.6:c.1717G=	ENSP00000414946.2:p.Ala573=
ENST00000562836.5:n.1971G=
ENST00000566510.5:c.*566G=	ENSP00000458139.1:n.*566G=
ENST00000566612.5:c.*140G=	ENSP00000454782.1:n.*140G=
ENST00000611625.4:c.1963G=	ENSP00000481063.1:p.Ala655=
ENST00000612417.4:c.1830+70G=	ENSP00000478360.1:n.1830+70G=
ENST00000621016.4:c.1865+35G=	ENSP00000480664.1:n.1865+35G=
NM_004360.3:c.1900G= , LRG_301t1:c.1900G=	NP_004351.1:p.Ala634=
XM_011523488.1:c.1165G=	XP_011521790.1:p.Ala389=
XM_011523489.1:c.1165G=	XP_011521791.1:p.Ala389=
NM_001317184.1:c.1717G=	NP_001304113.1:p.Ala573=
NM_001317185.1:c.352G=	NP_001304114.1:p.Ala118=
NM_001317186.1:c.-66G=	NP_001304115.1:n.-66G=
NM_004360.4:c.1900G=	NP_004351.1:p.Ala634=
NM_004360.5:c.1900G= MANE Select	NP_004351.1:p.Ala634=
NM_001317184.2:c.1717G=	NP_001304113.1:p.Ala573=
NM_001317185.2:c.352G=	NP_001304114.1:p.Ala118=
NM_001317186.2:c.-66G=	NP_001304115.1:n.-66G=