Canonical Allele Identifier: CA496152600

Gene: CDH1

Linked Data

• ClinVar Variation Id: 1561456
• ClinVar RCV Id: RCV002211840 ; RCV003303733
• dbSNP Id: rs2152126635
• MyVariant Identifiers: chr16:g.68835598A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68801695A>G , CM000678.2:g.68801695A>G	GRCh38
NC_000016.9:g.68835598A>G , CM000678.1:g.68835598A>G	GRCh37
NC_000016.8:g.67393099A>G	NCBI36
NG_008021.1:g.69404A>G , LRG_301:g.69404A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.189A>G MANE Select	ENSP00000261769.4:p.Arg63=
ENST00000261769.9:c.189A>G	ENSP00000261769.4:p.Arg63=
ENST00000422392.6:c.189A>G	ENSP00000414946.2:p.Arg63=
ENST00000562836.5:n.260A>G
ENST00000564676.5:n.471A>G
ENST00000564745.1:n.184A>G
ENST00000566510.5:c.189A>G	ENSP00000458139.1:p.Arg63=
ENST00000566612.5:c.189A>G	ENSP00000454782.1:p.Arg63=
ENST00000611625.4:c.189A>G	ENSP00000481063.1:p.Arg63=
ENST00000612417.4:c.189A>G	ENSP00000478360.1:p.Arg63=
ENST00000621016.4:c.189A>G	ENSP00000480664.1:p.Arg63=
NM_004360.3:c.189A>G , LRG_301t1:c.189A>G	NP_004351.1:p.Arg63=
XM_011523488.1:c.-547A>G	XP_011521790.1:n.-547A>G
XM_011523489.1:c.-547A>G	XP_011521791.1:n.-547A>G
NM_001317184.1:c.189A>G	NP_001304113.1:p.Arg63=
NM_001317185.1:c.-1427A>G	NP_001304114.1:n.-1427A>G
NM_001317186.1:c.-1631A>G	NP_001304115.1:n.-1631A>G
NM_004360.4:c.189A>G	NP_004351.1:p.Arg63=
NM_004360.5:c.189A>G MANE Select	NP_004351.1:p.Arg63=
NM_001317184.2:c.189A>G	NP_001304113.1:p.Arg63=
NM_001317185.2:c.-1427A>G	NP_001304114.1:n.-1427A>G
NM_001317186.2:c.-1631A>G	NP_001304115.1:n.-1631A>G