Canonical Allele Identifier: CA496393017

Gene: CDH1

Linked Data

• dbSNP Id: rs1057522719
• MyVariant Identifiers: chr16:g.68856109C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822206C>G , CM000678.2:g.68822206C>G	GRCh38
NC_000016.9:g.68856109C>G , CM000678.1:g.68856109C>G	GRCh37
NC_000016.8:g.67413610C>G	NCBI36
NG_008021.1:g.89915C>G , LRG_301:g.89915C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1917C>G MANE Select	ENSP00000261769.4:p.Thr639=
ENST00000261769.9:c.1917C>G	ENSP00000261769.4:p.Thr639=
ENST00000422392.6:c.1734C>G	ENSP00000414946.2:p.Thr578=
ENST00000562836.5:n.1988C>G
ENST00000566510.5:c.*583C>G	ENSP00000458139.1:n.*583C>G
ENST00000566612.5:c.*157C>G	ENSP00000454782.1:n.*157C>G
ENST00000611625.4:c.1980C>G	ENSP00000481063.1:p.Thr660=
ENST00000612417.4:c.1830+87C>G	ENSP00000478360.1:n.1830+87C>G
ENST00000621016.4:c.1865+52C>G	ENSP00000480664.1:n.1865+52C>G
NM_004360.3:c.1917C>G , LRG_301t1:c.1917C>G	NP_004351.1:p.Thr639=
XM_011523488.1:c.1182C>G	XP_011521790.1:p.Thr394=
XM_011523489.1:c.1182C>G	XP_011521791.1:p.Thr394=
NM_001317184.1:c.1734C>G	NP_001304113.1:p.Thr578=
NM_001317185.1:c.369C>G	NP_001304114.1:p.Thr123=
NM_001317186.1:c.-49C>G	NP_001304115.1:n.-49C>G
NM_004360.4:c.1917C>G	NP_004351.1:p.Thr639=
NM_004360.5:c.1917C>G MANE Select	NP_004351.1:p.Thr639=
NM_001317184.2:c.1734C>G	NP_001304113.1:p.Thr578=
NM_001317185.2:c.369C>G	NP_001304114.1:p.Thr123=
NM_001317186.2:c.-49C>G	NP_001304115.1:n.-49C>G