Canonical Allele Identifier: CA396467737

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68857410A>G (hg19) ; chr16:g.68823507A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823507A>G , CM000678.2:g.68823507A>G	GRCh38
NC_000016.9:g.68857410A>G , CM000678.1:g.68857410A>G	GRCh37
NC_000016.8:g.67414911A>G	NCBI36
NG_008021.1:g.91216A>G , LRG_301:g.91216A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2045A>G MANE Select	ENSP00000261769.4:p.Glu682Gly
ENST00000261769.9:c.2045A>G	ENSP00000261769.4:p.Glu682Gly
ENST00000422392.6:c.1862A>G	ENSP00000414946.2:p.Glu621Gly
ENST00000562118.1:n.263A>G
ENST00000562836.5:n.2116A>G
ENST00000566510.5:c.*711A>G	ENSP00000458139.1:n.*711A>G
ENST00000566612.5:c.*285A>G	ENSP00000454782.1:n.*285A>G
ENST00000611625.4:c.2108A>G	ENSP00000481063.1:p.Glu703Gly
ENST00000612417.4:c.1830+1388A>G	ENSP00000478360.1:n.1830+1388A>G
ENST00000621016.4:c.1865+1353A>G	ENSP00000480664.1:n.1865+1353A>G
NM_004360.3:c.2045A>G , LRG_301t1:c.2045A>G	NP_004351.1:p.Glu682Gly
XM_011523488.1:c.1310A>G	XP_011521790.1:p.Glu437Gly
XM_011523489.1:c.1310A>G	XP_011521791.1:p.Glu437Gly
NM_001317184.1:c.1862A>G	NP_001304113.1:p.Glu621Gly
NM_001317185.1:c.497A>G	NP_001304114.1:p.Glu166Gly
NM_001317186.1:c.80A>G	NP_001304115.1:p.Glu27Gly
NM_004360.4:c.2045A>G	NP_004351.1:p.Glu682Gly
NM_004360.5:c.2045A>G MANE Select	NP_004351.1:p.Glu682Gly
NM_001317184.2:c.1862A>G	NP_001304113.1:p.Glu621Gly
NM_001317185.2:c.497A>G	NP_001304114.1:p.Glu166Gly
NM_001317186.2:c.80A>G	NP_001304115.1:p.Glu27Gly