Canonical Allele Identifier: CA496392938

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68867195T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833292T>C , CM000678.2:g.68833292T>C	GRCh38
NC_000016.9:g.68867195T>C , CM000678.1:g.68867195T>C	GRCh37
NC_000016.8:g.67424696T>C	NCBI36
NG_008021.1:g.101001T>C , LRG_301:g.101001T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2442T>C MANE Select	ENSP00000261769.4:p.Asn814=
ENST00000261769.9:c.2442T>C	ENSP00000261769.4:p.Asn814=
ENST00000422392.6:c.2259T>C	ENSP00000414946.2:p.Asn753=
ENST00000562118.1:n.660T>C
ENST00000562836.5:n.2513T>C
ENST00000566510.5:c.*1108T>C	ENSP00000458139.1:n.*1108T>C
ENST00000566612.5:c.*682T>C	ENSP00000454782.1:n.*682T>C
ENST00000611625.4:c.2505T>C	ENSP00000481063.1:p.Asn835=
ENST00000612417.4:c.1854-899T>C	ENSP00000478360.1:n.1854-899T>C
ENST00000621016.4:c.1866-911T>C	ENSP00000480664.1:n.1866-911T>C
NM_004360.3:c.2442T>C , LRG_301t1:c.2442T>C	NP_004351.1:p.Asn814=
XM_011523488.1:c.1707T>C	XP_011521790.1:p.Asn569=
XM_011523489.1:c.1707T>C	XP_011521791.1:p.Asn569=
NM_001317184.1:c.2259T>C	NP_001304113.1:p.Asn753=
NM_001317185.1:c.894T>C	NP_001304114.1:p.Asn298=
NM_001317186.1:c.477T>C	NP_001304115.1:p.Asn159=
NM_004360.4:c.2442T>C	NP_004351.1:p.Asn814=
NM_004360.5:c.2442T>C MANE Select	NP_004351.1:p.Asn814=
NM_001317184.2:c.2259T>C	NP_001304113.1:p.Asn753=
NM_001317185.2:c.894T>C	NP_001304114.1:p.Asn298=
NM_001317186.2:c.477T>C	NP_001304115.1:p.Asn159=