Canonical Allele Identifier: CA396472501

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68867323A>C (hg19) ; chr16:g.68833420A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833420A>C , CM000678.2:g.68833420A>C	GRCh38
NC_000016.9:g.68867323A>C , CM000678.1:g.68867323A>C	GRCh37
NC_000016.8:g.67424824A>C	NCBI36
NG_008021.1:g.101129A>C , LRG_301:g.101129A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2570A>C MANE Select	ENSP00000261769.4:p.Gln857Pro
ENST00000261769.9:c.2570A>C	ENSP00000261769.4:p.Gln857Pro
ENST00000422392.6:c.2387A>C	ENSP00000414946.2:p.Gln796Pro
ENST00000562118.1:n.788A>C
ENST00000562836.5:n.2641A>C
ENST00000566510.5:c.*1236A>C	ENSP00000458139.1:n.*1236A>C
ENST00000566612.5:c.*810A>C	ENSP00000454782.1:n.*810A>C
ENST00000611625.4:c.2633A>C	ENSP00000481063.1:p.Gln878Pro
ENST00000612417.4:c.1854-771A>C	ENSP00000478360.1:n.1854-771A>C
ENST00000621016.4:c.1866-783A>C	ENSP00000480664.1:n.1866-783A>C
NM_004360.3:c.2570A>C , LRG_301t1:c.2570A>C	NP_004351.1:p.Gln857Pro
XM_011523488.1:c.1835A>C	XP_011521790.1:p.Gln612Pro
XM_011523489.1:c.1835A>C	XP_011521791.1:p.Gln612Pro
NM_001317184.1:c.2387A>C	NP_001304113.1:p.Gln796Pro
NM_001317185.1:c.1022A>C	NP_001304114.1:p.Gln341Pro
NM_001317186.1:c.605A>C	NP_001304115.1:p.Gln202Pro
NM_004360.4:c.2570A>C	NP_004351.1:p.Gln857Pro
NM_004360.5:c.2570A>C MANE Select	NP_004351.1:p.Gln857Pro
NM_001317184.2:c.2387A>C	NP_001304113.1:p.Gln796Pro
NM_001317185.2:c.1022A>C	NP_001304114.1:p.Gln341Pro
NM_001317186.2:c.605A>C	NP_001304115.1:p.Gln202Pro