Canonical Allele Identifier: CA396470875

Gene: CDH1

Linked Data

• dbSNP Id: rs150734856
• MyVariant Identifiers: chr16:g.68863583G>C (hg19) ; chr16:g.68829680G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829680G>C , CM000678.2:g.68829680G>C	GRCh38
NC_000016.9:g.68863583G>C , CM000678.1:g.68863583G>C	GRCh37
NC_000016.8:g.67421084G>C	NCBI36
NG_008021.1:g.97389G>C , LRG_301:g.97389G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2322G>C MANE Select	ENSP00000261769.4:p.Arg774Ser
ENST00000261769.9:c.2322G>C	ENSP00000261769.4:p.Arg774Ser
ENST00000422392.6:c.2139G>C	ENSP00000414946.2:p.Arg713Ser
ENST00000562118.1:n.540G>C
ENST00000562836.5:n.2393G>C
ENST00000566510.5:c.*988G>C	ENSP00000458139.1:n.*988G>C
ENST00000566612.5:c.*562G>C	ENSP00000454782.1:n.*562G>C
ENST00000611625.4:c.2385G>C	ENSP00000481063.1:p.Arg795Ser
ENST00000612417.4:c.1853+3126G>C	ENSP00000478360.1:n.1853+3126G>C
ENST00000621016.4:c.1866-4523G>C	ENSP00000480664.1:n.1866-4523G>C
NM_004360.3:c.2322G>C , LRG_301t1:c.2322G>C	NP_004351.1:p.Arg774Ser
XM_011523488.1:c.1587G>C	XP_011521790.1:p.Arg529Ser
XM_011523489.1:c.1587G>C	XP_011521791.1:p.Arg529Ser
NM_001317184.1:c.2139G>C	NP_001304113.1:p.Arg713Ser
NM_001317185.1:c.774G>C	NP_001304114.1:p.Arg258Ser
NM_001317186.1:c.357G>C	NP_001304115.1:p.Arg119Ser
NM_004360.4:c.2322G>C	NP_004351.1:p.Arg774Ser
NM_004360.5:c.2322G>C MANE Select	NP_004351.1:p.Arg774Ser
NM_001317184.2:c.2139G>C	NP_001304113.1:p.Arg713Ser
NM_001317185.2:c.774G>C	NP_001304114.1:p.Arg258Ser
NM_001317186.2:c.357G>C	NP_001304115.1:p.Arg119Ser