Canonical Allele Identifier: CA4448069

Gene: MET

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116700183A>G , CM000669.2:g.116700183A>G	GRCh38
NC_000007.13:g.116340237A>G , CM000669.1:g.116340237A>G	GRCh37
NC_000007.12:g.116127473A>G	NCBI36
NG_008996.1:g.32779A>G , LRG_662:g.32779A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.1099A>G	ENSP00000398776.2:p.Ile367Val
ENST00000436117.3:c.1099A>G	ENSP00000410980.2:p.Ile367Val
ENST00000318493.11:c.1099A>G	ENSP00000317272.6:p.Ile367Val
ENST00000397752.8:c.1099A>G MANE Select	ENSP00000380860.3:p.Ile367Val
ENST00000318493.10:c.1099A>G	ENSP00000317272.6:p.Ile367Val
ENST00000397752.7:c.1099A>G	ENSP00000380860.3:p.Ile367Val
ENST00000436117.2:c.1099A>G	ENSP00000410980.2:p.Ile367Val
NM_000245.2:c.1099A>G	NP_000236.2:p.Ile367Val
NM_001127500.1:c.1099A>G , LRG_662t1:c.1099A>G	NP_001120972.1:p.Ile367Val
XM_006715991.2:c.-91+27606A>G	XP_006716054.1:n.-91+27606A>G
XM_011516223.1:c.1156A>G	XP_011514525.1:p.Ile386Val
NM_000245.3:c.1099A>G	NP_000236.2:p.Ile367Val
NM_001127500.2:c.1099A>G	NP_001120972.1:p.Ile367Val
NM_001324401.1:c.1099A>G	NP_001311330.1:p.Ile367Val
NM_001324402.1:c.-91+27606A>G	NP_001311331.1:n.-91+27606A>G
XR_001744772.1:n.1330A>G
NM_001127500.3:c.1099A>G	NP_001120972.1:p.Ile367Val
NM_000245.4:c.1099A>G MANE Select	NP_000236.2:p.Ile367Val
NM_001324401.2:c.1099A>G	NP_001311330.1:p.Ile367Val
NM_001324402.2:c.-91+27606A>G	NP_001311331.1:n.-91+27606A>G
NM_001324401.3:c.1099A>G	NP_001311330.1:p.Ile367Val