Canonical Allele Identifier: CA2229979343

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68834088C= , CM000678.2:g.68834088C=	GRCh38
NC_000016.9:g.68867991C= , CM000678.1:g.68867991C=	GRCh37
NC_000016.8:g.67425492C=	NCBI36
NG_008021.1:g.101797C= , LRG_301:g.101797C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004360.5:c.*589C= MANE Select	NP_004351.1:n.*589C=
ENST00000261769.10:c.*589C= MANE Select	ENSP00000261769.4:n.*589C=
NM_001317184.1:c.*589C=	NP_001304113.1:n.*589C=
NM_001317184.2:c.*589C=	NP_001304113.1:n.*589C=
NM_001317185.1:c.*589C=	NP_001304114.1:n.*589C=
NM_001317185.2:c.*589C=	NP_001304114.1:n.*589C=
NM_001317186.1:c.*589C=	NP_001304115.1:n.*589C=
NM_001317186.2:c.*589C=	NP_001304115.1:n.*589C=
NM_004360.3:c.*589C= , LRG_301t1:c.*589C=	NP_004351.1:n.*589C=
NM_004360.4:c.*589C=	NP_004351.1:n.*589C=
ENST00000261769.9:c.*589C=	ENSP00000261769.4:n.*589C=
ENST00000566612.5:c.*1478C=	ENSP00000454782.1:n.*1478C=
ENST00000611625.4:c.*589C=	ENSP00000481063.1:n.*589C=
ENST00000612417.4:c.1854-103C=	ENSP00000478360.1:n.1854-103C=
ENST00000621016.4:c.1866-115C=	ENSP00000480664.1:n.1866-115C=
XM_011523488.1:c.*589C=	XP_011521790.1:n.*589C=
XM_011523489.1:c.*589C=	XP_011521791.1:n.*589C=