Canonical Allele Identifier: CA2732912077

Gene: CDH1

Linked Data

• dbSNP Id: rs2152144332

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833532T>A , CM000678.2:g.68833532T>A	GRCh38
NC_000016.9:g.68867435T>A , CM000678.1:g.68867435T>A	GRCh37
NC_000016.8:g.67424936T>A	NCBI36
NG_008021.1:g.101241T>A , LRG_301:g.101241T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.*33T>A MANE Select	ENSP00000261769.4:n.*33T>A
ENST00000261769.9:c.*33T>A	ENSP00000261769.4:n.*33T>A
ENST00000422392.6:c.*33T>A	ENSP00000414946.2:n.*33T>A
ENST00000562118.1:n.900T>A
ENST00000562836.5:n.2753T>A
ENST00000566510.5:c.*1348T>A	ENSP00000458139.1:n.*1348T>A
ENST00000566612.5:c.*922T>A	ENSP00000454782.1:n.*922T>A
ENST00000611625.4:c.*33T>A	ENSP00000481063.1:n.*33T>A
ENST00000612417.4:c.1854-659T>A	ENSP00000478360.1:n.1854-659T>A
ENST00000621016.4:c.1866-671T>A	ENSP00000480664.1:n.1866-671T>A
NM_004360.3:c.*33T>A , LRG_301t1:c.*33T>A	NP_004351.1:n.*33T>A
XM_011523488.1:c.*33T>A	XP_011521790.1:n.*33T>A
XM_011523489.1:c.*33T>A	XP_011521791.1:n.*33T>A
NM_001317184.1:c.*33T>A	NP_001304113.1:n.*33T>A
NM_001317185.1:c.*33T>A	NP_001304114.1:n.*33T>A
NM_001317186.1:c.*33T>A	NP_001304115.1:n.*33T>A
NM_004360.4:c.*33T>A	NP_004351.1:n.*33T>A
NM_004360.5:c.*33T>A MANE Select	NP_004351.1:n.*33T>A
NM_001317184.2:c.*33T>A	NP_001304113.1:n.*33T>A
NM_001317185.2:c.*33T>A	NP_001304114.1:n.*33T>A
NM_001317186.2:c.*33T>A	NP_001304115.1:n.*33T>A