Canonical Allele Identifier: CA2715553112

Gene: MET

Linked Data

• dbSNP Id: rs2116953234

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116763029del , CM000669.2:g.116763029del	GRCh38
NC_000007.13:g.116403083del , CM000669.1:g.116403083del	GRCh37
NC_000007.12:g.116190319del	NCBI36
NG_008996.1:g.95625del , LRG_662:g.95625del

Transcript Alleles

HGVS	Amino-acid change
ENST00000422097.2:c.2365-21del	ENSP00000398776.2:n.2365-21del
ENST00000436117.3:c.2265-21del	ENSP00000410980.2:n.2265-21del
ENST00000318493.11:c.2419-21del	ENSP00000317272.6:n.2419-21del
ENST00000397752.8:c.2365-21del MANE Select	ENSP00000380860.3:n.2365-21del
ENST00000318493.10:c.2419-21del	ENSP00000317272.6:n.2419-21del
ENST00000397752.7:c.2365-21del	ENSP00000380860.3:n.2365-21del
ENST00000422097.1:c.205-21del	ENSP00000398776.1:n.205-21del
ENST00000436117.2:c.2265-21del	ENSP00000410980.2:n.2265-21del
NM_000245.2:c.2365-21del	NP_000236.2:n.2365-21del
NM_001127500.1:c.2419-21del , LRG_662t1:c.2419-21del	NP_001120972.1:n.2419-21del
XM_006715990.2:c.1075-21del	XP_006716053.1:n.1075-21del
XM_006715991.2:c.1075-21del	XP_006716054.1:n.1075-21del
XM_011516223.1:c.2422-21del	XP_011514525.1:n.2422-21del
NM_000245.3:c.2365-21del	NP_000236.2:n.2365-21del
NM_001127500.2:c.2419-21del	NP_001120972.1:n.2419-21del
NM_001324401.1:c.2365-21del	NP_001311330.1:n.2365-21del
NM_001324402.1:c.1075-21del	NP_001311331.1:n.1075-21del
XR_001744772.1:n.2496-21del
NM_001127500.3:c.2419-21del	NP_001120972.1:n.2419-21del
NM_000245.4:c.2365-21del MANE Select	NP_000236.2:n.2365-21del
NM_001324401.2:c.2365-21del	NP_001311330.1:n.2365-21del
NM_001324402.2:c.1075-21del	NP_001311331.1:n.1075-21del
NM_001324401.3:c.2365-21del	NP_001311330.1:n.2365-21del