Canonical Allele Identifier: CA496393068

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68857336C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823433C>G , CM000678.2:g.68823433C>G	GRCh38
NC_000016.9:g.68857336C>G , CM000678.1:g.68857336C>G	GRCh37
NC_000016.8:g.67414837C>G	NCBI36
NG_008021.1:g.91142C>G , LRG_301:g.91142C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1971C>G MANE Select	ENSP00000261769.4:p.Ala657=
ENST00000261769.9:c.1971C>G	ENSP00000261769.4:p.Ala657=
ENST00000422392.6:c.1788C>G	ENSP00000414946.2:p.Ala596=
ENST00000562118.1:n.189C>G
ENST00000562836.5:n.2042C>G
ENST00000566510.5:c.*637C>G	ENSP00000458139.1:n.*637C>G
ENST00000566612.5:c.*211C>G	ENSP00000454782.1:n.*211C>G
ENST00000611625.4:c.2034C>G	ENSP00000481063.1:p.Ala678=
ENST00000612417.4:c.1830+1314C>G	ENSP00000478360.1:n.1830+1314C>G
ENST00000621016.4:c.1865+1279C>G	ENSP00000480664.1:n.1865+1279C>G
NM_004360.3:c.1971C>G , LRG_301t1:c.1971C>G	NP_004351.1:p.Ala657=
XM_011523488.1:c.1236C>G	XP_011521790.1:p.Ala412=
XM_011523489.1:c.1236C>G	XP_011521791.1:p.Ala412=
NM_001317184.1:c.1788C>G	NP_001304113.1:p.Ala596=
NM_001317185.1:c.423C>G	NP_001304114.1:p.Ala141=
NM_001317186.1:c.6C>G	NP_001304115.1:p.Ala2=
NM_004360.4:c.1971C>G	NP_004351.1:p.Ala657=
NM_004360.5:c.1971C>G MANE Select	NP_004351.1:p.Ala657=
NM_001317184.2:c.1788C>G	NP_001304113.1:p.Ala596=
NM_001317185.2:c.423C>G	NP_001304114.1:p.Ala141=
NM_001317186.2:c.6C>G	NP_001304115.1:p.Ala2=