Canonical Allele Identifier: CA396470734

Gene: CDH1

Linked Data

• dbSNP Id: rs2152142208
• MyVariant Identifiers: chr16:g.68863558A>T (hg19) ; chr16:g.68829655A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829655A>T , CM000678.2:g.68829655A>T	GRCh38
NC_000016.9:g.68863558A>T , CM000678.1:g.68863558A>T	GRCh37
NC_000016.8:g.67421059A>T	NCBI36
NG_008021.1:g.97364A>T , LRG_301:g.97364A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2297A>T MANE Select	ENSP00000261769.4:p.Asp766Val
ENST00000261769.9:c.2297A>T	ENSP00000261769.4:p.Asp766Val
ENST00000422392.6:c.2114A>T	ENSP00000414946.2:p.Asp705Val
ENST00000562118.1:n.515A>T
ENST00000562836.5:n.2368A>T
ENST00000566510.5:c.*963A>T	ENSP00000458139.1:n.*963A>T
ENST00000566612.5:c.*537A>T	ENSP00000454782.1:n.*537A>T
ENST00000611625.4:c.2360A>T	ENSP00000481063.1:p.Asp787Val
ENST00000612417.4:c.1853+3101A>T	ENSP00000478360.1:n.1853+3101A>T
ENST00000621016.4:c.1866-4548A>T	ENSP00000480664.1:n.1866-4548A>T
NM_004360.3:c.2297A>T , LRG_301t1:c.2297A>T	NP_004351.1:p.Asp766Val
XM_011523488.1:c.1562A>T	XP_011521790.1:p.Asp521Val
XM_011523489.1:c.1562A>T	XP_011521791.1:p.Asp521Val
NM_001317184.1:c.2114A>T	NP_001304113.1:p.Asp705Val
NM_001317185.1:c.749A>T	NP_001304114.1:p.Asp250Val
NM_001317186.1:c.332A>T	NP_001304115.1:p.Asp111Val
NM_004360.4:c.2297A>T	NP_004351.1:p.Asp766Val
NM_004360.5:c.2297A>T MANE Select	NP_004351.1:p.Asp766Val
NM_001317184.2:c.2114A>T	NP_001304113.1:p.Asp705Val
NM_001317185.2:c.749A>T	NP_001304114.1:p.Asp250Val
NM_001317186.2:c.332A>T	NP_001304115.1:p.Asp111Val