Canonical Allele Identifier: CA396470820

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68863572C>A (hg19) ; chr16:g.68829669C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829669C>A , CM000678.2:g.68829669C>A	GRCh38
NC_000016.9:g.68863572C>A , CM000678.1:g.68863572C>A	GRCh37
NC_000016.8:g.67421073C>A	NCBI36
NG_008021.1:g.97378C>A , LRG_301:g.97378C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2311C>A MANE Select	ENSP00000261769.4:p.Gln771Lys
ENST00000261769.9:c.2311C>A	ENSP00000261769.4:p.Gln771Lys
ENST00000422392.6:c.2128C>A	ENSP00000414946.2:p.Gln710Lys
ENST00000562118.1:n.529C>A
ENST00000562836.5:n.2382C>A
ENST00000566510.5:c.*977C>A	ENSP00000458139.1:n.*977C>A
ENST00000566612.5:c.*551C>A	ENSP00000454782.1:n.*551C>A
ENST00000611625.4:c.2374C>A	ENSP00000481063.1:p.Gln792Lys
ENST00000612417.4:c.1853+3115C>A	ENSP00000478360.1:n.1853+3115C>A
ENST00000621016.4:c.1866-4534C>A	ENSP00000480664.1:n.1866-4534C>A
NM_004360.3:c.2311C>A , LRG_301t1:c.2311C>A	NP_004351.1:p.Gln771Lys
XM_011523488.1:c.1576C>A	XP_011521790.1:p.Gln526Lys
XM_011523489.1:c.1576C>A	XP_011521791.1:p.Gln526Lys
NM_001317184.1:c.2128C>A	NP_001304113.1:p.Gln710Lys
NM_001317185.1:c.763C>A	NP_001304114.1:p.Gln255Lys
NM_001317186.1:c.346C>A	NP_001304115.1:p.Gln116Lys
NM_004360.4:c.2311C>A	NP_004351.1:p.Gln771Lys
NM_004360.5:c.2311C>A MANE Select	NP_004351.1:p.Gln771Lys
NM_001317184.2:c.2128C>A	NP_001304113.1:p.Gln710Lys
NM_001317185.2:c.763C>A	NP_001304114.1:p.Gln255Lys
NM_001317186.2:c.346C>A	NP_001304115.1:p.Gln116Lys