Canonical Allele Identifier: CA396467619

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68857357A>C (hg19) ; chr16:g.68823454A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68823454A>C , CM000678.2:g.68823454A>C	GRCh38
NC_000016.9:g.68857357A>C , CM000678.1:g.68857357A>C	GRCh37
NC_000016.8:g.67414858A>C	NCBI36
NG_008021.1:g.91163A>C , LRG_301:g.91163A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1992A>C MANE Select	ENSP00000261769.4:p.Lys664Asn
ENST00000261769.9:c.1992A>C	ENSP00000261769.4:p.Lys664Asn
ENST00000422392.6:c.1809A>C	ENSP00000414946.2:p.Lys603Asn
ENST00000562118.1:n.210A>C
ENST00000562836.5:n.2063A>C
ENST00000566510.5:c.*658A>C	ENSP00000458139.1:n.*658A>C
ENST00000566612.5:c.*232A>C	ENSP00000454782.1:n.*232A>C
ENST00000611625.4:c.2055A>C	ENSP00000481063.1:p.Lys685Asn
ENST00000612417.4:c.1830+1335A>C	ENSP00000478360.1:n.1830+1335A>C
ENST00000621016.4:c.1865+1300A>C	ENSP00000480664.1:n.1865+1300A>C
NM_004360.3:c.1992A>C , LRG_301t1:c.1992A>C	NP_004351.1:p.Lys664Asn
XM_011523488.1:c.1257A>C	XP_011521790.1:p.Lys419Asn
XM_011523489.1:c.1257A>C	XP_011521791.1:p.Lys419Asn
NM_001317184.1:c.1809A>C	NP_001304113.1:p.Lys603Asn
NM_001317185.1:c.444A>C	NP_001304114.1:p.Lys148Asn
NM_001317186.1:c.27A>C	NP_001304115.1:p.Lys9Asn
NM_004360.4:c.1992A>C	NP_004351.1:p.Lys664Asn
NM_004360.5:c.1992A>C MANE Select	NP_004351.1:p.Lys664Asn
NM_001317184.2:c.1809A>C	NP_001304113.1:p.Lys603Asn
NM_001317185.2:c.444A>C	NP_001304114.1:p.Lys148Asn
NM_001317186.2:c.27A>C	NP_001304115.1:p.Lys9Asn