Canonical Allele Identifier: CA496393008

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68856103C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822200C>T , CM000678.2:g.68822200C>T	GRCh38
NC_000016.9:g.68856103C>T , CM000678.1:g.68856103C>T	GRCh37
NC_000016.8:g.67413604C>T	NCBI36
NG_008021.1:g.89909C>T , LRG_301:g.89909C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1911C>T MANE Select	ENSP00000261769.4:p.Asn637=
ENST00000261769.9:c.1911C>T	ENSP00000261769.4:p.Asn637=
ENST00000422392.6:c.1728C>T	ENSP00000414946.2:p.Asn576=
ENST00000562836.5:n.1982C>T
ENST00000566510.5:c.*577C>T	ENSP00000458139.1:n.*577C>T
ENST00000566612.5:c.*151C>T	ENSP00000454782.1:n.*151C>T
ENST00000611625.4:c.1974C>T	ENSP00000481063.1:p.Asn658=
ENST00000612417.4:c.1830+81C>T	ENSP00000478360.1:n.1830+81C>T
ENST00000621016.4:c.1865+46C>T	ENSP00000480664.1:n.1865+46C>T
NM_004360.3:c.1911C>T , LRG_301t1:c.1911C>T	NP_004351.1:p.Asn637=
XM_011523488.1:c.1176C>T	XP_011521790.1:p.Asn392=
XM_011523489.1:c.1176C>T	XP_011521791.1:p.Asn392=
NM_001317184.1:c.1728C>T	NP_001304113.1:p.Asn576=
NM_001317185.1:c.363C>T	NP_001304114.1:p.Asn121=
NM_001317186.1:c.-55C>T	NP_001304115.1:n.-55C>T
NM_004360.4:c.1911C>T	NP_004351.1:p.Asn637=
NM_004360.5:c.1911C>T MANE Select	NP_004351.1:p.Asn637=
NM_001317184.2:c.1728C>T	NP_001304113.1:p.Asn576=
NM_001317185.2:c.363C>T	NP_001304114.1:p.Asn121=
NM_001317186.2:c.-55C>T	NP_001304115.1:n.-55C>T