Canonical Allele Identifier: CA496392569

Gene: CDH1

Linked Data

• dbSNP Id: rs2152138310
• MyVariant Identifiers: chr16:g.68855986A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822083A>T , CM000678.2:g.68822083A>T	GRCh38
NC_000016.9:g.68855986A>T , CM000678.1:g.68855986A>T	GRCh37
NC_000016.8:g.67413487A>T	NCBI36
NG_008021.1:g.89792A>T , LRG_301:g.89792A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1794A>T MANE Select	ENSP00000261769.4:p.Arg598=
ENST00000261769.9:c.1794A>T	ENSP00000261769.4:p.Arg598=
ENST00000422392.6:c.1611A>T	ENSP00000414946.2:p.Arg537=
ENST00000562836.5:n.1865A>T
ENST00000566510.5:c.*460A>T	ENSP00000458139.1:n.*460A>T
ENST00000566612.5:c.*34A>T	ENSP00000454782.1:n.*34A>T
ENST00000611625.4:c.1857A>T	ENSP00000481063.1:p.Arg619=
ENST00000612417.4:c.1794A>T	ENSP00000478360.1:p.Arg598=
ENST00000621016.4:c.1794A>T	ENSP00000480664.1:p.Arg598=
NM_004360.3:c.1794A>T , LRG_301t1:c.1794A>T	NP_004351.1:p.Arg598=
XM_011523488.1:c.1059A>T	XP_011521790.1:p.Arg353=
XM_011523489.1:c.1059A>T	XP_011521791.1:p.Arg353=
NM_001317184.1:c.1611A>T	NP_001304113.1:p.Arg537=
NM_001317185.1:c.246A>T	NP_001304114.1:p.Arg82=
NM_001317186.1:c.-172A>T	NP_001304115.1:n.-172A>T
NM_004360.4:c.1794A>T	NP_004351.1:p.Arg598=
NM_004360.5:c.1794A>T MANE Select	NP_004351.1:p.Arg598=
NM_001317184.2:c.1611A>T	NP_001304113.1:p.Arg537=
NM_001317185.2:c.246A>T	NP_001304114.1:p.Arg82=
NM_001317186.2:c.-172A>T	NP_001304115.1:n.-172A>T