Canonical Allele Identifier: CA396467224

Gene: CDH1

Linked Data

• dbSNP Id: rs755482251
• MyVariant Identifiers: chr16:g.68856102A>C (hg19) ; chr16:g.68822199A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822199A>C , CM000678.2:g.68822199A>C	GRCh38
NC_000016.9:g.68856102A>C , CM000678.1:g.68856102A>C	GRCh37
NC_000016.8:g.67413603A>C	NCBI36
NG_008021.1:g.89908A>C , LRG_301:g.89908A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.1910A>C MANE Select	ENSP00000261769.4:p.Asn637Thr
ENST00000261769.9:c.1910A>C	ENSP00000261769.4:p.Asn637Thr
ENST00000422392.6:c.1727A>C	ENSP00000414946.2:p.Asn576Thr
ENST00000562836.5:n.1981A>C
ENST00000566510.5:c.*576A>C	ENSP00000458139.1:n.*576A>C
ENST00000566612.5:c.*150A>C	ENSP00000454782.1:n.*150A>C
ENST00000611625.4:c.1973A>C	ENSP00000481063.1:p.Asn658Thr
ENST00000612417.4:c.1830+80A>C	ENSP00000478360.1:n.1830+80A>C
ENST00000621016.4:c.1865+45A>C	ENSP00000480664.1:n.1865+45A>C
NM_004360.3:c.1910A>C , LRG_301t1:c.1910A>C	NP_004351.1:p.Asn637Thr
XM_011523488.1:c.1175A>C	XP_011521790.1:p.Asn392Thr
XM_011523489.1:c.1175A>C	XP_011521791.1:p.Asn392Thr
NM_001317184.1:c.1727A>C	NP_001304113.1:p.Asn576Thr
NM_001317185.1:c.362A>C	NP_001304114.1:p.Asn121Thr
NM_001317186.1:c.-56A>C	NP_001304115.1:n.-56A>C
NM_004360.4:c.1910A>C	NP_004351.1:p.Asn637Thr
NM_004360.5:c.1910A>C MANE Select	NP_004351.1:p.Asn637Thr
NM_001317184.2:c.1727A>C	NP_001304113.1:p.Asn576Thr
NM_001317185.2:c.362A>C	NP_001304114.1:p.Asn121Thr
NM_001317186.2:c.-56A>C	NP_001304115.1:n.-56A>C