Canonical Allele Identifier: CA645567311

Gene: MET

Linked Data

• dbSNP Id: rs2116998047
• COSMIC: COSM24687 ; COSM29633 ; COSM88794 ; COSM5574327

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771990del , CM000669.2:g.116771990del	GRCh38
NC_000007.13:g.116412044del , CM000669.1:g.116412044del	GRCh37
NC_000007.12:g.116199280del	NCBI36
NG_008996.1:g.104586del , LRG_662:g.104586del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*633+1del
ENST00000318493.11:c.3082+1del
ENST00000397752.8:c.3028+1del
ENST00000318493.10:c.3082+1del
ENST00000397752.7:c.3028+1del
ENST00000454623.1:c.283+336del	ENSP00000398140.1:n.283+336del
NM_000245.2:c.3028+1del
NM_001127500.1:c.3082+1del , LRG_662t1:c.3082+1del
XM_006715990.2:c.1738+1del
XM_006715991.2:c.1738+1del
XM_011516223.1:c.3085+1del
NM_000245.3:c.3028+1del
NM_001127500.2:c.3082+1del
NM_001324402.1:c.1738+1del
XR_001744772.1:n.3159+1del
NM_001127500.3:c.3082+1del
NM_000245.4:c.3028+1del
NM_001324402.2:c.1738+1del