Canonical Allele Identifier: CA396471406

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68863700A>C (hg19) ; chr16:g.68829797A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829797A>C , CM000678.2:g.68829797A>C	GRCh38
NC_000016.9:g.68863700A>C , CM000678.1:g.68863700A>C	GRCh37
NC_000016.8:g.67421201A>C	NCBI36
NG_008021.1:g.97506A>C , LRG_301:g.97506A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2439A>C MANE Select	ENSP00000261769.4:p.Glu813Asp
ENST00000261769.9:c.2439A>C	ENSP00000261769.4:p.Glu813Asp
ENST00000422392.6:c.2256A>C	ENSP00000414946.2:p.Glu752Asp
ENST00000562118.1:n.657A>C
ENST00000562836.5:n.2510A>C
ENST00000566510.5:c.*1105A>C	ENSP00000458139.1:n.*1105A>C
ENST00000566612.5:c.*679A>C	ENSP00000454782.1:n.*679A>C
ENST00000611625.4:c.2502A>C	ENSP00000481063.1:p.Glu834Asp
ENST00000612417.4:c.1853+3243A>C	ENSP00000478360.1:n.1853+3243A>C
ENST00000621016.4:c.1866-4406A>C	ENSP00000480664.1:n.1866-4406A>C
NM_004360.3:c.2439A>C , LRG_301t1:c.2439A>C	NP_004351.1:p.Glu813Asp
XM_011523488.1:c.1704A>C	XP_011521790.1:p.Glu568Asp
XM_011523489.1:c.1704A>C	XP_011521791.1:p.Glu568Asp
NM_001317184.1:c.2256A>C	NP_001304113.1:p.Glu752Asp
NM_001317185.1:c.891A>C	NP_001304114.1:p.Glu297Asp
NM_001317186.1:c.474A>C	NP_001304115.1:p.Glu158Asp
NM_004360.4:c.2439A>C	NP_004351.1:p.Glu813Asp
NM_004360.5:c.2439A>C MANE Select	NP_004351.1:p.Glu813Asp
NM_001317184.2:c.2256A>C	NP_001304113.1:p.Glu752Asp
NM_001317185.2:c.891A>C	NP_001304114.1:p.Glu297Asp
NM_001317186.2:c.474A>C	NP_001304115.1:p.Glu158Asp