Canonical Allele Identifier: CA2580612869

Gene: CDH1

Linked Data

• ClinVar Variation Id: 2502928
• ClinVar RCV Id: RCV003229662

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68811208_68812850del , CM000678.2:g.68811208_68812850del	GRCh38
NC_000016.9:g.68845111_68846753del , CM000678.1:g.68845111_68846753del	GRCh37
NC_000016.8:g.67402612_67404254del	NCBI36
NG_008021.1:g.78917_80559del , LRG_301:g.78917_80559del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.833-476_1138-463del
ENST00000261769.9:c.833-476_1138-463del
ENST00000422392.6:c.833-476_1137+587del
ENST00000562836.5:n.904-476_1209-463del
ENST00000566510.5:c.677-476_982-463del
ENST00000566612.5:c.833-476_1138-463del
ENST00000611625.4:c.833-476_1138-463del
ENST00000612417.4:c.833-476_1138-463del
ENST00000621016.4:c.833-476_1138-463del
NM_004360.3:c.833-476_1138-463del , LRG_301t1:c.833-476_1138-463del
XM_011523488.1:c.98-476_403-463del
XM_011523489.1:c.98-476_403-463del
NM_001317184.1:c.833-476_1137+587del
NM_001317185.1:c.-783-476_-478-463del
NM_001317186.1:c.-987-476_-682-463del
NM_004360.4:c.833-476_1138-463del
NM_004360.5:c.833-476_1138-463del
NM_001317184.2:c.833-476_1137+587del
NM_001317185.2:c.-783-476_-478-463del
NM_001317186.2:c.-987-476_-682-463del