Canonical Allele Identifier: CA396463044

Gene: CDH1

Linked Data

• dbSNP Id: rs2152134924
• MyVariant Identifiers: chr16:g.68849542A>G (hg19) ; chr16:g.68815639A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815639A>G , CM000678.2:g.68815639A>G	GRCh38
NC_000016.9:g.68849542A>G , CM000678.1:g.68849542A>G	GRCh37
NC_000016.8:g.67407043A>G	NCBI36
NG_008021.1:g.83348A>G , LRG_301:g.83348A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1445A>G MANE Select	ENSP00000261769.4:p.Glu482Gly
ENST00000261769.9:c.1445A>G	ENSP00000261769.4:p.Glu482Gly
ENST00000422392.6:c.1262A>G	ENSP00000414946.2:p.Glu421Gly
ENST00000562836.5:n.1516A>G
ENST00000566510.5:c.*111A>G	ENSP00000458139.1:n.*111A>G
ENST00000566612.5:c.1445A>G	ENSP00000454782.1:p.Glu482Gly
ENST00000611625.4:c.1508A>G	ENSP00000481063.1:p.Glu503Gly
ENST00000612417.4:c.1445A>G	ENSP00000478360.1:p.Glu482Gly
ENST00000621016.4:c.1445A>G	ENSP00000480664.1:p.Glu482Gly
NM_004360.3:c.1445A>G , LRG_301t1:c.1445A>G	NP_004351.1:p.Glu482Gly
XM_011523488.1:c.710A>G	XP_011521790.1:p.Glu237Gly
XM_011523489.1:c.710A>G	XP_011521791.1:p.Glu237Gly
NM_001317184.1:c.1262A>G	NP_001304113.1:p.Glu421Gly
NM_001317185.1:c.-104A>G	NP_001304114.1:n.-104A>G
NM_001317186.1:c.-375A>G	NP_001304115.1:n.-375A>G
NM_004360.4:c.1445A>G	NP_004351.1:p.Glu482Gly
NM_004360.5:c.1445A>G MANE Select	NP_004351.1:p.Glu482Gly
NM_001317184.2:c.1262A>G	NP_001304113.1:p.Glu421Gly
NM_001317185.2:c.-104A>G	NP_001304114.1:n.-104A>G
NM_001317186.2:c.-375A>G	NP_001304115.1:n.-375A>G