Canonical Allele Identifier: CA2582342561

Gene: CDH1

Linked Data

• ClinVar Variation Id: 2587431
• ClinVar RCV Id: RCV003344135 ; RCV003512214

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68808445_68808446delinsAG , CM000678.2:g.68808445_68808446delinsAG	GRCh38
NC_000016.9:g.68842348_68842349delinsAG , CM000678.1:g.68842348_68842349delinsAG	GRCh37
NC_000016.8:g.67399849_67399850delinsAG	NCBI36
NG_008021.1:g.76154_76155delinsAG , LRG_301:g.76154_76155delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.409_410delinsAG MANE Select	ENSP00000261769.4:p.Ala137Arg
ENST00000261769.9:c.409_410delinsAG	ENSP00000261769.4:p.Ala137Arg
ENST00000422392.6:c.409_410delinsAG	ENSP00000414946.2:p.Ala137Arg
ENST00000561751.1:c.176_177delinsAG
ENST00000562836.5:n.480_481delinsAG
ENST00000564676.5:n.691_692delinsAG
ENST00000564745.1:n.404_405delinsAG
ENST00000566510.5:c.409_410delinsAG	ENSP00000458139.1:p.Ala137Arg
ENST00000566612.5:c.409_410delinsAG	ENSP00000454782.1:p.Ala137Arg
ENST00000611625.4:c.409_410delinsAG	ENSP00000481063.1:p.Ala137Arg
ENST00000612417.4:c.409_410delinsAG	ENSP00000478360.1:p.Ala137Arg
ENST00000621016.4:c.409_410delinsAG	ENSP00000480664.1:p.Ala137Arg
NM_004360.3:c.409_410delinsAG , LRG_301t1:c.409_410delinsAG	NP_004351.1:p.Ala137Arg
XM_011523488.1:c.-327_-326delinsAG	XP_011521790.1:n.-327_-326delinsAG
XM_011523489.1:c.-327_-326delinsAG	XP_011521791.1:n.-327_-326delinsAG
NM_001317184.1:c.409_410delinsAG	NP_001304113.1:p.Ala137Arg
NM_001317185.1:c.-1207_-1206delinsAG	NP_001304114.1:n.-1207_-1206delinsAG
NM_001317186.1:c.-1411_-1410delinsAG	NP_001304115.1:n.-1411_-1410delinsAG
NM_004360.4:c.409_410delinsAG	NP_004351.1:p.Ala137Arg
NM_004360.5:c.409_410delinsAG MANE Select	NP_004351.1:p.Ala137Arg
NM_001317184.2:c.409_410delinsAG	NP_001304113.1:p.Ala137Arg
NM_001317185.2:c.-1207_-1206delinsAG	NP_001304114.1:n.-1207_-1206delinsAG
NM_001317186.2:c.-1411_-1410delinsAG	NP_001304115.1:n.-1411_-1410delinsAG