Canonical Allele Identifier: CA396470912

Gene: CDH1

Linked Data

• dbSNP Id: rs372989292
• MyVariant Identifiers: chr16:g.68863590G>C (hg19) ; chr16:g.68829687G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829687G>C , CM000678.2:g.68829687G>C	GRCh38
NC_000016.9:g.68863590G>C , CM000678.1:g.68863590G>C	GRCh37
NC_000016.8:g.67421091G>C	NCBI36
NG_008021.1:g.97396G>C , LRG_301:g.97396G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2329G>C MANE Select	ENSP00000261769.4:p.Asp777His
ENST00000261769.9:c.2329G>C	ENSP00000261769.4:p.Asp777His
ENST00000422392.6:c.2146G>C	ENSP00000414946.2:p.Asp716His
ENST00000562118.1:n.547G>C
ENST00000562836.5:n.2400G>C
ENST00000566510.5:c.*995G>C	ENSP00000458139.1:n.*995G>C
ENST00000566612.5:c.*569G>C	ENSP00000454782.1:n.*569G>C
ENST00000611625.4:c.2392G>C	ENSP00000481063.1:p.Asp798His
ENST00000612417.4:c.1853+3133G>C	ENSP00000478360.1:n.1853+3133G>C
ENST00000621016.4:c.1866-4516G>C	ENSP00000480664.1:n.1866-4516G>C
NM_004360.3:c.2329G>C , LRG_301t1:c.2329G>C	NP_004351.1:p.Asp777His
XM_011523488.1:c.1594G>C	XP_011521790.1:p.Asp532His
XM_011523489.1:c.1594G>C	XP_011521791.1:p.Asp532His
NM_001317184.1:c.2146G>C	NP_001304113.1:p.Asp716His
NM_001317185.1:c.781G>C	NP_001304114.1:p.Asp261His
NM_001317186.1:c.364G>C	NP_001304115.1:p.Asp122His
NM_004360.4:c.2329G>C	NP_004351.1:p.Asp777His
NM_004360.5:c.2329G>C MANE Select	NP_004351.1:p.Asp777His
NM_001317184.2:c.2146G>C	NP_001304113.1:p.Asp716His
NM_001317185.2:c.781G>C	NP_001304114.1:p.Asp261His
NM_001317186.2:c.364G>C	NP_001304115.1:p.Asp122His