Canonical Allele Identifier: CA283312885

Gene: CDH1

Linked Data

• dbSNP Id: rs879189193
• MyVariant Identifiers: chr16:g.68857339A>G (hg19) ; chr16:g.68823436A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823436A>G , CM000678.2:g.68823436A>G	GRCh38
NC_000016.9:g.68857339A>G , CM000678.1:g.68857339A>G	GRCh37
NC_000016.8:g.67414840A>G	NCBI36
NG_008021.1:g.91145A>G , LRG_301:g.91145A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1974A>G MANE Select	ENSP00000261769.4:p.Leu658=
ENST00000261769.9:c.1974A>G	ENSP00000261769.4:p.Leu658=
ENST00000422392.6:c.1791A>G	ENSP00000414946.2:p.Leu597=
ENST00000562118.1:n.192A>G
ENST00000562836.5:n.2045A>G
ENST00000566510.5:c.*640A>G	ENSP00000458139.1:n.*640A>G
ENST00000566612.5:c.*214A>G	ENSP00000454782.1:n.*214A>G
ENST00000611625.4:c.2037A>G	ENSP00000481063.1:p.Leu679=
ENST00000612417.4:c.1830+1317A>G	ENSP00000478360.1:n.1830+1317A>G
ENST00000621016.4:c.1865+1282A>G	ENSP00000480664.1:n.1865+1282A>G
NM_004360.3:c.1974A>G , LRG_301t1:c.1974A>G	NP_004351.1:p.Leu658=
XM_011523488.1:c.1239A>G	XP_011521790.1:p.Leu413=
XM_011523489.1:c.1239A>G	XP_011521791.1:p.Leu413=
NM_001317184.1:c.1791A>G	NP_001304113.1:p.Leu597=
NM_001317185.1:c.426A>G	NP_001304114.1:p.Leu142=
NM_001317186.1:c.9A>G	NP_001304115.1:p.Leu3=
NM_004360.4:c.1974A>G	NP_004351.1:p.Leu658=
NM_004360.5:c.1974A>G MANE Select	NP_004351.1:p.Leu658=
NM_001317184.2:c.1791A>G	NP_001304113.1:p.Leu597=
NM_001317185.2:c.426A>G	NP_001304114.1:p.Leu142=
NM_001317186.2:c.9A>G	NP_001304115.1:p.Leu3=