Canonical Allele Identifier: CA496392591

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68856010T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822107T>C , CM000678.2:g.68822107T>C	GRCh38
NC_000016.9:g.68856010T>C , CM000678.1:g.68856010T>C	GRCh37
NC_000016.8:g.67413511T>C	NCBI36
NG_008021.1:g.89816T>C , LRG_301:g.89816T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1818T>C MANE Select	ENSP00000261769.4:p.Asn606=
ENST00000261769.9:c.1818T>C	ENSP00000261769.4:p.Asn606=
ENST00000422392.6:c.1635T>C	ENSP00000414946.2:p.Asn545=
ENST00000562836.5:n.1889T>C
ENST00000566510.5:c.*484T>C	ENSP00000458139.1:n.*484T>C
ENST00000566612.5:c.*58T>C	ENSP00000454782.1:n.*58T>C
ENST00000611625.4:c.1881T>C	ENSP00000481063.1:p.Asn627=
ENST00000612417.4:c.1818T>C	ENSP00000478360.1:p.Asn606=
ENST00000621016.4:c.1818T>C	ENSP00000480664.1:p.Asn606=
NM_004360.3:c.1818T>C , LRG_301t1:c.1818T>C	NP_004351.1:p.Asn606=
XM_011523488.1:c.1083T>C	XP_011521790.1:p.Asn361=
XM_011523489.1:c.1083T>C	XP_011521791.1:p.Asn361=
NM_001317184.1:c.1635T>C	NP_001304113.1:p.Asn545=
NM_001317185.1:c.270T>C	NP_001304114.1:p.Asn90=
NM_001317186.1:c.-148T>C	NP_001304115.1:n.-148T>C
NM_004360.4:c.1818T>C	NP_004351.1:p.Asn606=
NM_004360.5:c.1818T>C MANE Select	NP_004351.1:p.Asn606=
NM_001317184.2:c.1635T>C	NP_001304113.1:p.Asn545=
NM_001317185.2:c.270T>C	NP_001304114.1:p.Asn90=
NM_001317186.2:c.-148T>C	NP_001304115.1:n.-148T>C