Canonical Allele Identifier: CA283319785

Gene: CDH1

Linked Data

• dbSNP Id: rs2229044
• MyVariant Identifiers: chr16:g.68867387C>G (hg19) ; chr16:g.68833484C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833484C>G , CM000678.2:g.68833484C>G	GRCh38
NC_000016.9:g.68867387C>G , CM000678.1:g.68867387C>G	GRCh37
NC_000016.8:g.67424888C>G	NCBI36
NG_008021.1:g.101193C>G , LRG_301:g.101193C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2634C>G MANE Select	ENSP00000261769.4:p.Gly878=
ENST00000261769.9:c.2634C>G	ENSP00000261769.4:p.Gly878=
ENST00000422392.6:c.2451C>G	ENSP00000414946.2:p.Gly817=
ENST00000562118.1:n.852C>G
ENST00000562836.5:n.2705C>G
ENST00000566510.5:c.*1300C>G	ENSP00000458139.1:n.*1300C>G
ENST00000566612.5:c.*874C>G	ENSP00000454782.1:n.*874C>G
ENST00000611625.4:c.2697C>G	ENSP00000481063.1:p.Gly899=
ENST00000612417.4:c.1854-707C>G	ENSP00000478360.1:n.1854-707C>G
ENST00000621016.4:c.1866-719C>G	ENSP00000480664.1:n.1866-719C>G
NM_004360.3:c.2634C>G , LRG_301t1:c.2634C>G	NP_004351.1:p.Gly878=
XM_011523488.1:c.1899C>G	XP_011521790.1:p.Gly633=
XM_011523489.1:c.1899C>G	XP_011521791.1:p.Gly633=
NM_001317184.1:c.2451C>G	NP_001304113.1:p.Gly817=
NM_001317185.1:c.1086C>G	NP_001304114.1:p.Gly362=
NM_001317186.1:c.669C>G	NP_001304115.1:p.Gly223=
NM_004360.4:c.2634C>G	NP_004351.1:p.Gly878=
NM_004360.5:c.2634C>G MANE Select	NP_004351.1:p.Gly878=
NM_001317184.2:c.2451C>G	NP_001304113.1:p.Gly817=
NM_001317185.2:c.1086C>G	NP_001304114.1:p.Gly362=
NM_001317186.2:c.669C>G	NP_001304115.1:p.Gly223=