Canonical Allele Identifier: CA396463041

Gene: CDH1

Linked Data

• dbSNP Id: rs1555516138
• MyVariant Identifiers: chr16:g.68849541G>C (hg19) ; chr16:g.68815638G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815638G>C , CM000678.2:g.68815638G>C	GRCh38
NC_000016.9:g.68849541G>C , CM000678.1:g.68849541G>C	GRCh37
NC_000016.8:g.67407042G>C	NCBI36
NG_008021.1:g.83347G>C , LRG_301:g.83347G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1444G>C MANE Select	ENSP00000261769.4:p.Glu482Gln
ENST00000261769.9:c.1444G>C	ENSP00000261769.4:p.Glu482Gln
ENST00000422392.6:c.1261G>C	ENSP00000414946.2:p.Glu421Gln
ENST00000562836.5:n.1515G>C
ENST00000566510.5:c.*110G>C	ENSP00000458139.1:n.*110G>C
ENST00000566612.5:c.1444G>C	ENSP00000454782.1:p.Glu482Gln
ENST00000611625.4:c.1507G>C	ENSP00000481063.1:p.Glu503Gln
ENST00000612417.4:c.1444G>C	ENSP00000478360.1:p.Glu482Gln
ENST00000621016.4:c.1444G>C	ENSP00000480664.1:p.Glu482Gln
NM_004360.3:c.1444G>C , LRG_301t1:c.1444G>C	NP_004351.1:p.Glu482Gln
XM_011523488.1:c.709G>C	XP_011521790.1:p.Glu237Gln
XM_011523489.1:c.709G>C	XP_011521791.1:p.Glu237Gln
NM_001317184.1:c.1261G>C	NP_001304113.1:p.Glu421Gln
NM_001317185.1:c.-105G>C	NP_001304114.1:n.-105G>C
NM_001317186.1:c.-376G>C	NP_001304115.1:n.-376G>C
NM_004360.4:c.1444G>C	NP_004351.1:p.Glu482Gln
NM_004360.5:c.1444G>C MANE Select	NP_004351.1:p.Glu482Gln
NM_001317184.2:c.1261G>C	NP_001304113.1:p.Glu421Gln
NM_001317185.2:c.-105G>C	NP_001304114.1:n.-105G>C
NM_001317186.2:c.-376G>C	NP_001304115.1:n.-376G>C