Canonical Allele Identifier: CA396466480

Gene: CDH1

Linked Data

• dbSNP Id: rs864622599
• MyVariant Identifiers: chr16:g.68855949C>G (hg19) ; chr16:g.68822046C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822046C>G , CM000678.2:g.68822046C>G	GRCh38
NC_000016.9:g.68855949C>G , CM000678.1:g.68855949C>G	GRCh37
NC_000016.8:g.67413450C>G	NCBI36
NG_008021.1:g.89755C>G , LRG_301:g.89755C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1757C>G MANE Select	ENSP00000261769.4:p.Ser586Cys
ENST00000261769.9:c.1757C>G	ENSP00000261769.4:p.Ser586Cys
ENST00000422392.6:c.1574C>G	ENSP00000414946.2:p.Ser525Cys
ENST00000562836.5:n.1828C>G
ENST00000566510.5:c.*423C>G	ENSP00000458139.1:n.*423C>G
ENST00000566612.5:c.1611C>G	ENSP00000454782.1:p.Val537=
ENST00000611625.4:c.1820C>G	ENSP00000481063.1:p.Ser607Cys
ENST00000612417.4:c.1757C>G	ENSP00000478360.1:p.Ser586Cys
ENST00000621016.4:c.1757C>G	ENSP00000480664.1:p.Ser586Cys
NM_004360.3:c.1757C>G , LRG_301t1:c.1757C>G	NP_004351.1:p.Ser586Cys
XM_011523488.1:c.1022C>G	XP_011521790.1:p.Ser341Cys
XM_011523489.1:c.1022C>G	XP_011521791.1:p.Ser341Cys
NM_001317184.1:c.1574C>G	NP_001304113.1:p.Ser525Cys
NM_001317185.1:c.209C>G	NP_001304114.1:p.Ser70Cys
NM_001317186.1:c.-209C>G	NP_001304115.1:n.-209C>G
NM_004360.4:c.1757C>G	NP_004351.1:p.Ser586Cys
NM_004360.5:c.1757C>G MANE Select	NP_004351.1:p.Ser586Cys
NM_001317184.2:c.1574C>G	NP_001304113.1:p.Ser525Cys
NM_001317185.2:c.209C>G	NP_001304114.1:p.Ser70Cys
NM_001317186.2:c.-209C>G	NP_001304115.1:n.-209C>G