Canonical Allele Identifier: CA496393217

Gene: CDH1

Linked Data

• dbSNP Id: rs2152144182
• MyVariant Identifiers: chr16:g.68867360C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833457C>T , CM000678.2:g.68833457C>T	GRCh38
NC_000016.9:g.68867360C>T , CM000678.1:g.68867360C>T	GRCh37
NC_000016.8:g.67424861C>T	NCBI36
NG_008021.1:g.101166C>T , LRG_301:g.101166C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2607C>T MANE Select	ENSP00000261769.4:p.Phe869=
ENST00000261769.9:c.2607C>T	ENSP00000261769.4:p.Phe869=
ENST00000422392.6:c.2424C>T	ENSP00000414946.2:p.Phe808=
ENST00000562118.1:n.825C>T
ENST00000562836.5:n.2678C>T
ENST00000566510.5:c.*1273C>T	ENSP00000458139.1:n.*1273C>T
ENST00000566612.5:c.*847C>T	ENSP00000454782.1:n.*847C>T
ENST00000611625.4:c.2670C>T	ENSP00000481063.1:p.Phe890=
ENST00000612417.4:c.1854-734C>T	ENSP00000478360.1:n.1854-734C>T
ENST00000621016.4:c.1866-746C>T	ENSP00000480664.1:n.1866-746C>T
NM_004360.3:c.2607C>T , LRG_301t1:c.2607C>T	NP_004351.1:p.Phe869=
XM_011523488.1:c.1872C>T	XP_011521790.1:p.Phe624=
XM_011523489.1:c.1872C>T	XP_011521791.1:p.Phe624=
NM_001317184.1:c.2424C>T	NP_001304113.1:p.Phe808=
NM_001317185.1:c.1059C>T	NP_001304114.1:p.Phe353=
NM_001317186.1:c.642C>T	NP_001304115.1:p.Phe214=
NM_004360.4:c.2607C>T	NP_004351.1:p.Phe869=
NM_004360.5:c.2607C>T MANE Select	NP_004351.1:p.Phe869=
NM_001317184.2:c.2424C>T	NP_001304113.1:p.Phe808=
NM_001317185.2:c.1059C>T	NP_001304114.1:p.Phe353=
NM_001317186.2:c.642C>T	NP_001304115.1:p.Phe214=