Canonical Allele Identifier: CA496154398

Gene: CDH1

Linked Data

• ClinVar Variation Id: 1777181
• ClinVar RCV Id: RCV002395002 ; RCV003512172
• MyVariant Identifiers: chr16:g.68853265A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68819362A>C , CM000678.2:g.68819362A>C	GRCh38
NC_000016.9:g.68853265A>C , CM000678.1:g.68853265A>C	GRCh37
NC_000016.8:g.67410766A>C	NCBI36
NG_008021.1:g.87071A>C , LRG_301:g.87071A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1648A>C MANE Select	ENSP00000261769.4:p.Arg550=
ENST00000261769.9:c.1648A>C	ENSP00000261769.4:p.Arg550=
ENST00000422392.6:c.1465A>C	ENSP00000414946.2:p.Arg489=
ENST00000562836.5:n.1719A>C
ENST00000566510.5:c.*314A>C	ENSP00000458139.1:n.*314A>C
ENST00000566612.5:c.1566-2639A>C	ENSP00000454782.1:n.1566-2639A>C
ENST00000611625.4:c.1711A>C	ENSP00000481063.1:p.Arg571=
ENST00000612417.4:c.1648A>C	ENSP00000478360.1:p.Arg550=
ENST00000621016.4:c.1648A>C	ENSP00000480664.1:p.Arg550=
NM_004360.3:c.1648A>C , LRG_301t1:c.1648A>C	NP_004351.1:p.Arg550=
XM_011523488.1:c.913A>C	XP_011521790.1:p.Arg305=
XM_011523489.1:c.913A>C	XP_011521791.1:p.Arg305=
NM_001317184.1:c.1465A>C	NP_001304113.1:p.Arg489=
NM_001317185.1:c.100A>C	NP_001304114.1:p.Arg34=
NM_001317186.1:c.-254-2639A>C	NP_001304115.1:n.-254-2639A>C
NM_004360.4:c.1648A>C	NP_004351.1:p.Arg550=
NM_004360.5:c.1648A>C MANE Select	NP_004351.1:p.Arg550=
NM_001317184.2:c.1465A>C	NP_001304113.1:p.Arg489=
NM_001317185.2:c.100A>C	NP_001304114.1:p.Arg34=
NM_001317186.2:c.-254-2639A>C	NP_001304115.1:n.-254-2639A>C