Canonical Allele Identifier: CA396458958

Gene: CDH1

Linked Data

• dbSNP Id: rs1555515468
• MyVariant Identifiers: chr16:g.68844231A>T (hg19) ; chr16:g.68810328A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810328A>T , CM000678.2:g.68810328A>T	GRCh38
NC_000016.9:g.68844231A>T , CM000678.1:g.68844231A>T	GRCh37
NC_000016.8:g.67401732A>T	NCBI36
NG_008021.1:g.78037A>T , LRG_301:g.78037A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.819A>T MANE Select	ENSP00000261769.4:p.Glu273Asp
ENST00000261769.9:c.819A>T	ENSP00000261769.4:p.Glu273Asp
ENST00000422392.6:c.819A>T	ENSP00000414946.2:p.Glu273Asp
ENST00000561751.1:c.455-1356A>T
ENST00000562836.5:n.890A>T
ENST00000566510.5:c.663A>T	ENSP00000458139.1:p.Glu221Asp
ENST00000566612.5:c.819A>T	ENSP00000454782.1:p.Glu273Asp
ENST00000611625.4:c.819A>T	ENSP00000481063.1:p.Glu273Asp
ENST00000612417.4:c.819A>T	ENSP00000478360.1:p.Glu273Asp
ENST00000621016.4:c.819A>T	ENSP00000480664.1:p.Glu273Asp
NM_004360.3:c.819A>T , LRG_301t1:c.819A>T	NP_004351.1:p.Glu273Asp
XM_011523488.1:c.84A>T	XP_011521790.1:p.Glu28Asp
XM_011523489.1:c.84A>T	XP_011521791.1:p.Glu28Asp
NM_001317184.1:c.819A>T	NP_001304113.1:p.Glu273Asp
NM_001317185.1:c.-797A>T	NP_001304114.1:n.-797A>T
NM_001317186.1:c.-1001A>T	NP_001304115.1:n.-1001A>T
NM_004360.4:c.819A>T	NP_004351.1:p.Glu273Asp
NM_004360.5:c.819A>T MANE Select	NP_004351.1:p.Glu273Asp
NM_001317184.2:c.819A>T	NP_001304113.1:p.Glu273Asp
NM_001317185.2:c.-797A>T	NP_001304114.1:n.-797A>T
NM_001317186.2:c.-1001A>T	NP_001304115.1:n.-1001A>T