Canonical Allele Identifier: CA283312021

Gene: CDH1

Linked Data

• dbSNP Id: rs1044050273
• MyVariant Identifiers: chr16:g.68855991T>C (hg19) ; chr16:g.68822088T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68822088T>C , CM000678.2:g.68822088T>C	GRCh38
NC_000016.9:g.68855991T>C , CM000678.1:g.68855991T>C	GRCh37
NC_000016.8:g.67413492T>C	NCBI36
NG_008021.1:g.89797T>C , LRG_301:g.89797T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1799T>C MANE Select	ENSP00000261769.4:p.Ile600Thr
ENST00000261769.9:c.1799T>C	ENSP00000261769.4:p.Ile600Thr
ENST00000422392.6:c.1616T>C	ENSP00000414946.2:p.Ile539Thr
ENST00000562836.5:n.1870T>C
ENST00000566510.5:c.*465T>C	ENSP00000458139.1:n.*465T>C
ENST00000566612.5:c.*39T>C	ENSP00000454782.1:n.*39T>C
ENST00000611625.4:c.1862T>C	ENSP00000481063.1:p.Ile621Thr
ENST00000612417.4:c.1799T>C	ENSP00000478360.1:p.Ile600Thr
ENST00000621016.4:c.1799T>C	ENSP00000480664.1:p.Ile600Thr
NM_004360.3:c.1799T>C , LRG_301t1:c.1799T>C	NP_004351.1:p.Ile600Thr
XM_011523488.1:c.1064T>C	XP_011521790.1:p.Ile355Thr
XM_011523489.1:c.1064T>C	XP_011521791.1:p.Ile355Thr
NM_001317184.1:c.1616T>C	NP_001304113.1:p.Ile539Thr
NM_001317185.1:c.251T>C	NP_001304114.1:p.Ile84Thr
NM_001317186.1:c.-167T>C	NP_001304115.1:n.-167T>C
NM_004360.4:c.1799T>C	NP_004351.1:p.Ile600Thr
NM_004360.5:c.1799T>C MANE Select	NP_004351.1:p.Ile600Thr
NM_001317184.2:c.1616T>C	NP_001304113.1:p.Ile539Thr
NM_001317185.2:c.251T>C	NP_001304114.1:p.Ile84Thr
NM_001317186.2:c.-167T>C	NP_001304115.1:n.-167T>C