Canonical Allele Identifier: CA2732921701

Gene: CDH1

Linked Data

• dbSNP Id: rs2152129864

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68808588_68808595del , CM000678.2:g.68808588_68808595del	GRCh38
NC_000016.9:g.68842491_68842498del , CM000678.1:g.68842491_68842498del	GRCh37
NC_000016.8:g.67399992_67399999del	NCBI36
NG_008021.1:g.76297_76304del , LRG_301:g.76297_76304del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.531+21_531+28del MANE Select	ENSP00000261769.4:n.531+21_531+28del
ENST00000261769.9:c.531+21_531+28del	ENSP00000261769.4:n.531+21_531+28del
ENST00000422392.6:c.531+21_531+28del	ENSP00000414946.2:n.531+21_531+28del
ENST00000561751.1:c.298+21_298+28del
ENST00000562836.5:n.602+21_602+28del
ENST00000564676.5:n.813+21_813+28del
ENST00000564745.1:n.526+21_526+28del
ENST00000566510.5:c.531+21_531+28del	ENSP00000458139.1:n.531+21_531+28del
ENST00000566612.5:c.531+21_531+28del	ENSP00000454782.1:n.531+21_531+28del
ENST00000567320.1:n.41+21_41+28del
ENST00000611625.4:c.531+21_531+28del	ENSP00000481063.1:n.531+21_531+28del
ENST00000612417.4:c.531+21_531+28del	ENSP00000478360.1:n.531+21_531+28del
ENST00000621016.4:c.531+21_531+28del	ENSP00000480664.1:n.531+21_531+28del
NM_004360.3:c.531+21_531+28del , LRG_301t1:c.531+21_531+28del	NP_004351.1:n.531+21_531+28del
XM_011523488.1:c.-205+21_-205+28del	XP_011521790.1:n.-205+21_-205+28del
XM_011523489.1:c.-205+21_-205+28del	XP_011521791.1:n.-205+21_-205+28del
NM_001317184.1:c.531+21_531+28del	NP_001304113.1:n.531+21_531+28del
NM_001317185.1:c.-1085+21_-1085+28del	NP_001304114.1:n.-1085+21_-1085+28del
NM_001317186.1:c.-1289+21_-1289+28del	NP_001304115.1:n.-1289+21_-1289+28del
NM_004360.4:c.531+21_531+28del	NP_004351.1:n.531+21_531+28del
NM_004360.5:c.531+21_531+28del MANE Select	NP_004351.1:n.531+21_531+28del
NM_001317184.2:c.531+21_531+28del	NP_001304113.1:n.531+21_531+28del
NM_001317185.2:c.-1085+21_-1085+28del	NP_001304114.1:n.-1085+21_-1085+28del
NM_001317186.2:c.-1289+21_-1289+28del	NP_001304115.1:n.-1289+21_-1289+28del