Canonical Allele Identifier: CA496157495

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68863664T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829761T>G , CM000678.2:g.68829761T>G	GRCh38
NC_000016.9:g.68863664T>G , CM000678.1:g.68863664T>G	GRCh37
NC_000016.8:g.67421165T>G	NCBI36
NG_008021.1:g.97470T>G , LRG_301:g.97470T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2403T>G MANE Select	ENSP00000261769.4:p.Pro801=
ENST00000261769.9:c.2403T>G	ENSP00000261769.4:p.Pro801=
ENST00000422392.6:c.2220T>G	ENSP00000414946.2:p.Pro740=
ENST00000562118.1:n.621T>G
ENST00000562836.5:n.2474T>G
ENST00000566510.5:c.*1069T>G	ENSP00000458139.1:n.*1069T>G
ENST00000566612.5:c.*643T>G	ENSP00000454782.1:n.*643T>G
ENST00000611625.4:c.2466T>G	ENSP00000481063.1:p.Pro822=
ENST00000612417.4:c.1853+3207T>G	ENSP00000478360.1:n.1853+3207T>G
ENST00000621016.4:c.1866-4442T>G	ENSP00000480664.1:n.1866-4442T>G
NM_004360.3:c.2403T>G , LRG_301t1:c.2403T>G	NP_004351.1:p.Pro801=
XM_011523488.1:c.1668T>G	XP_011521790.1:p.Pro556=
XM_011523489.1:c.1668T>G	XP_011521791.1:p.Pro556=
NM_001317184.1:c.2220T>G	NP_001304113.1:p.Pro740=
NM_001317185.1:c.855T>G	NP_001304114.1:p.Pro285=
NM_001317186.1:c.438T>G	NP_001304115.1:p.Pro146=
NM_004360.4:c.2403T>G	NP_004351.1:p.Pro801=
NM_004360.5:c.2403T>G MANE Select	NP_004351.1:p.Pro801=
NM_001317184.2:c.2220T>G	NP_001304113.1:p.Pro740=
NM_001317185.2:c.855T>G	NP_001304114.1:p.Pro285=
NM_001317186.2:c.438T>G	NP_001304115.1:p.Pro146=