Canonical Allele Identifier: CA396467059

Gene: CDH1

Linked Data

• gnomAD v4: 16-68822154-A-C
• MyVariant Identifiers: chr16:g.68856057A>C (hg19) ; chr16:g.68822154A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822154A>C , CM000678.2:g.68822154A>C	GRCh38
NC_000016.9:g.68856057A>C , CM000678.1:g.68856057A>C	GRCh37
NC_000016.8:g.67413558A>C	NCBI36
NG_008021.1:g.89863A>C , LRG_301:g.89863A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1865A>C MANE Select	ENSP00000261769.4:p.Asn622Thr
ENST00000261769.9:c.1865A>C	ENSP00000261769.4:p.Asn622Thr
ENST00000422392.6:c.1682A>C	ENSP00000414946.2:p.Asn561Thr
ENST00000562836.5:n.1936A>C
ENST00000566510.5:c.*531A>C	ENSP00000458139.1:n.*531A>C
ENST00000566612.5:c.*105A>C	ENSP00000454782.1:n.*105A>C
ENST00000611625.4:c.1928A>C	ENSP00000481063.1:p.Asn643Thr
ENST00000612417.4:c.1830+35A>C	ENSP00000478360.1:n.1830+35A>C
ENST00000621016.4:c.1865A>C	ENSP00000480664.1:p.Asn622Thr
NM_004360.3:c.1865A>C , LRG_301t1:c.1865A>C	NP_004351.1:p.Asn622Thr
XM_011523488.1:c.1130A>C	XP_011521790.1:p.Asn377Thr
XM_011523489.1:c.1130A>C	XP_011521791.1:p.Asn377Thr
NM_001317184.1:c.1682A>C	NP_001304113.1:p.Asn561Thr
NM_001317185.1:c.317A>C	NP_001304114.1:p.Asn106Thr
NM_001317186.1:c.-101A>C	NP_001304115.1:n.-101A>C
NM_004360.4:c.1865A>C	NP_004351.1:p.Asn622Thr
NM_004360.5:c.1865A>C MANE Select	NP_004351.1:p.Asn622Thr
NM_001317184.2:c.1682A>C	NP_001304113.1:p.Asn561Thr
NM_001317185.2:c.317A>C	NP_001304114.1:p.Asn106Thr
NM_001317186.2:c.-101A>C	NP_001304115.1:n.-101A>C