Canonical Allele Identifier: CA396459733

Gene: CDH1

Linked Data

• dbSNP Id: rs529089668
• MyVariant Identifiers: chr16:g.68845680C>A (hg19) ; chr16:g.68811777C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68811777C>A , CM000678.2:g.68811777C>A	GRCh38
NC_000016.9:g.68845680C>A , CM000678.1:g.68845680C>A	GRCh37
NC_000016.8:g.67403181C>A	NCBI36
NG_008021.1:g.79486C>A , LRG_301:g.79486C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.926C>A MANE Select	ENSP00000261769.4:p.Pro309His
ENST00000261769.9:c.926C>A	ENSP00000261769.4:p.Pro309His
ENST00000422392.6:c.926C>A	ENSP00000414946.2:p.Pro309His
ENST00000561751.1:c.548C>A
ENST00000562836.5:n.997C>A
ENST00000566510.5:c.770C>A	ENSP00000458139.1:p.Pro257His
ENST00000566612.5:c.926C>A	ENSP00000454782.1:p.Pro309His
ENST00000611625.4:c.926C>A	ENSP00000481063.1:p.Pro309His
ENST00000612417.4:c.926C>A	ENSP00000478360.1:p.Pro309His
ENST00000621016.4:c.926C>A	ENSP00000480664.1:p.Pro309His
NM_004360.3:c.926C>A , LRG_301t1:c.926C>A	NP_004351.1:p.Pro309His
XM_011523488.1:c.191C>A	XP_011521790.1:p.Pro64His
XM_011523489.1:c.191C>A	XP_011521791.1:p.Pro64His
NM_001317184.1:c.926C>A	NP_001304113.1:p.Pro309His
NM_001317185.1:c.-690C>A	NP_001304114.1:n.-690C>A
NM_001317186.1:c.-894C>A	NP_001304115.1:n.-894C>A
NM_004360.4:c.926C>A	NP_004351.1:p.Pro309His
NM_004360.5:c.926C>A MANE Select	NP_004351.1:p.Pro309His
NM_001317184.2:c.926C>A	NP_001304113.1:p.Pro309His
NM_001317185.2:c.-690C>A	NP_001304114.1:n.-690C>A
NM_001317186.2:c.-894C>A	NP_001304115.1:n.-894C>A