Canonical Allele Identifier: CA496393082

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68867264A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833361A>G , CM000678.2:g.68833361A>G	GRCh38
NC_000016.9:g.68867264A>G , CM000678.1:g.68867264A>G	GRCh37
NC_000016.8:g.67424765A>G	NCBI36
NG_008021.1:g.101070A>G , LRG_301:g.101070A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2511A>G MANE Select	ENSP00000261769.4:p.Gly837=
ENST00000261769.9:c.2511A>G	ENSP00000261769.4:p.Gly837=
ENST00000422392.6:c.2328A>G	ENSP00000414946.2:p.Gly776=
ENST00000562118.1:n.729A>G
ENST00000562836.5:n.2582A>G
ENST00000566510.5:c.*1177A>G	ENSP00000458139.1:n.*1177A>G
ENST00000566612.5:c.*751A>G	ENSP00000454782.1:n.*751A>G
ENST00000611625.4:c.2574A>G	ENSP00000481063.1:p.Gly858=
ENST00000612417.4:c.1854-830A>G	ENSP00000478360.1:n.1854-830A>G
ENST00000621016.4:c.1866-842A>G	ENSP00000480664.1:n.1866-842A>G
NM_004360.3:c.2511A>G , LRG_301t1:c.2511A>G	NP_004351.1:p.Gly837=
XM_011523488.1:c.1776A>G	XP_011521790.1:p.Gly592=
XM_011523489.1:c.1776A>G	XP_011521791.1:p.Gly592=
NM_001317184.1:c.2328A>G	NP_001304113.1:p.Gly776=
NM_001317185.1:c.963A>G	NP_001304114.1:p.Gly321=
NM_001317186.1:c.546A>G	NP_001304115.1:p.Gly182=
NM_004360.4:c.2511A>G	NP_004351.1:p.Gly837=
NM_004360.5:c.2511A>G MANE Select	NP_004351.1:p.Gly837=
NM_001317184.2:c.2328A>G	NP_001304113.1:p.Gly776=
NM_001317185.2:c.963A>G	NP_001304114.1:p.Gly321=
NM_001317186.2:c.546A>G	NP_001304115.1:p.Gly182=