Canonical Allele Identifier: CA396472243

Gene: CDH1

Linked Data

• dbSNP Id: rs1961536737
• MyVariant Identifiers: chr16:g.68867263G>T (hg19) ; chr16:g.68833360G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833360G>T , CM000678.2:g.68833360G>T	GRCh38
NC_000016.9:g.68867263G>T , CM000678.1:g.68867263G>T	GRCh37
NC_000016.8:g.67424764G>T	NCBI36
NG_008021.1:g.101069G>T , LRG_301:g.101069G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2510G>T MANE Select	ENSP00000261769.4:p.Gly837Val
ENST00000261769.9:c.2510G>T	ENSP00000261769.4:p.Gly837Val
ENST00000422392.6:c.2327G>T	ENSP00000414946.2:p.Gly776Val
ENST00000562118.1:n.728G>T
ENST00000562836.5:n.2581G>T
ENST00000566510.5:c.*1176G>T	ENSP00000458139.1:n.*1176G>T
ENST00000566612.5:c.*750G>T	ENSP00000454782.1:n.*750G>T
ENST00000611625.4:c.2573G>T	ENSP00000481063.1:p.Gly858Val
ENST00000612417.4:c.1854-831G>T	ENSP00000478360.1:n.1854-831G>T
ENST00000621016.4:c.1866-843G>T	ENSP00000480664.1:n.1866-843G>T
NM_004360.3:c.2510G>T , LRG_301t1:c.2510G>T	NP_004351.1:p.Gly837Val
XM_011523488.1:c.1775G>T	XP_011521790.1:p.Gly592Val
XM_011523489.1:c.1775G>T	XP_011521791.1:p.Gly592Val
NM_001317184.1:c.2327G>T	NP_001304113.1:p.Gly776Val
NM_001317185.1:c.962G>T	NP_001304114.1:p.Gly321Val
NM_001317186.1:c.545G>T	NP_001304115.1:p.Gly182Val
NM_004360.4:c.2510G>T	NP_004351.1:p.Gly837Val
NM_004360.5:c.2510G>T MANE Select	NP_004351.1:p.Gly837Val
NM_001317184.2:c.2327G>T	NP_001304113.1:p.Gly776Val
NM_001317185.2:c.962G>T	NP_001304114.1:p.Gly321Val
NM_001317186.2:c.545G>T	NP_001304115.1:p.Gly182Val