Canonical Allele Identifier: CA496393098

Gene: CDH1

Linked Data

• dbSNP Id: rs2152143996
• MyVariant Identifiers: chr16:g.68867279T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833376T>G , CM000678.2:g.68833376T>G	GRCh38
NC_000016.9:g.68867279T>G , CM000678.1:g.68867279T>G	GRCh37
NC_000016.8:g.67424780T>G	NCBI36
NG_008021.1:g.101085T>G , LRG_301:g.101085T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2526T>G MANE Select	ENSP00000261769.4:p.Ala842=
ENST00000261769.9:c.2526T>G	ENSP00000261769.4:p.Ala842=
ENST00000422392.6:c.2343T>G	ENSP00000414946.2:p.Ala781=
ENST00000562118.1:n.744T>G
ENST00000562836.5:n.2597T>G
ENST00000566510.5:c.*1192T>G	ENSP00000458139.1:n.*1192T>G
ENST00000566612.5:c.*766T>G	ENSP00000454782.1:n.*766T>G
ENST00000611625.4:c.2589T>G	ENSP00000481063.1:p.Ala863=
ENST00000612417.4:c.1854-815T>G	ENSP00000478360.1:n.1854-815T>G
ENST00000621016.4:c.1866-827T>G	ENSP00000480664.1:n.1866-827T>G
NM_004360.3:c.2526T>G , LRG_301t1:c.2526T>G	NP_004351.1:p.Ala842=
XM_011523488.1:c.1791T>G	XP_011521790.1:p.Ala597=
XM_011523489.1:c.1791T>G	XP_011521791.1:p.Ala597=
NM_001317184.1:c.2343T>G	NP_001304113.1:p.Ala781=
NM_001317185.1:c.978T>G	NP_001304114.1:p.Ala326=
NM_001317186.1:c.561T>G	NP_001304115.1:p.Ala187=
NM_004360.4:c.2526T>G	NP_004351.1:p.Ala842=
NM_004360.5:c.2526T>G MANE Select	NP_004351.1:p.Ala842=
NM_001317184.2:c.2343T>G	NP_001304113.1:p.Ala781=
NM_001317185.2:c.978T>G	NP_001304114.1:p.Ala326=
NM_001317186.2:c.561T>G	NP_001304115.1:p.Ala187=