Canonical Allele Identifier: CA396472661

Gene: CDH1

Linked Data

• dbSNP Id: rs864622630
• MyVariant Identifiers: chr16:g.68867355C>G (hg19) ; chr16:g.68833452C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833452C>G , CM000678.2:g.68833452C>G	GRCh38
NC_000016.9:g.68867355C>G , CM000678.1:g.68867355C>G	GRCh37
NC_000016.8:g.67424856C>G	NCBI36
NG_008021.1:g.101161C>G , LRG_301:g.101161C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2602C>G MANE Select	ENSP00000261769.4:p.Arg868Gly
ENST00000261769.9:c.2602C>G	ENSP00000261769.4:p.Arg868Gly
ENST00000422392.6:c.2419C>G	ENSP00000414946.2:p.Arg807Gly
ENST00000562118.1:n.820C>G
ENST00000562836.5:n.2673C>G
ENST00000566510.5:c.*1268C>G	ENSP00000458139.1:n.*1268C>G
ENST00000566612.5:c.*842C>G	ENSP00000454782.1:n.*842C>G
ENST00000611625.4:c.2665C>G	ENSP00000481063.1:p.Arg889Gly
ENST00000612417.4:c.1854-739C>G	ENSP00000478360.1:n.1854-739C>G
ENST00000621016.4:c.1866-751C>G	ENSP00000480664.1:n.1866-751C>G
NM_004360.3:c.2602C>G , LRG_301t1:c.2602C>G	NP_004351.1:p.Arg868Gly
XM_011523488.1:c.1867C>G	XP_011521790.1:p.Arg623Gly
XM_011523489.1:c.1867C>G	XP_011521791.1:p.Arg623Gly
NM_001317184.1:c.2419C>G	NP_001304113.1:p.Arg807Gly
NM_001317185.1:c.1054C>G	NP_001304114.1:p.Arg352Gly
NM_001317186.1:c.637C>G	NP_001304115.1:p.Arg213Gly
NM_004360.4:c.2602C>G	NP_004351.1:p.Arg868Gly
NM_004360.5:c.2602C>G MANE Select	NP_004351.1:p.Arg868Gly
NM_001317184.2:c.2419C>G	NP_001304113.1:p.Arg807Gly
NM_001317185.2:c.1054C>G	NP_001304114.1:p.Arg352Gly
NM_001317186.2:c.637C>G	NP_001304115.1:p.Arg213Gly