Canonical Allele Identifier: CA1737029721
Gene: MET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116763229G= , CM000669.2:g.116763229G= GRCh38
NC_000007.13:g.116403283G= , CM000669.1:g.116403283G= GRCh37
NC_000007.12:g.116190519G= NCBI36
NG_008996.1:g.95825G= , LRG_662:g.95825G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000422097.2:c.2544G= ENSP00000398776.2:p.Val848=
ENST00000436117.3:c.*149G= ENSP00000410980.2:n.*149G=
ENST00000318493.11:c.2598G= ENSP00000317272.6:p.Val866=
ENST00000397752.8:c.2544G= MANE Select ENSP00000380860.3:p.Val848=
ENST00000318493.10:c.2598G= ENSP00000317272.6:p.Val866=
ENST00000397752.7:c.2544G= ENSP00000380860.3:p.Val848=
ENST00000422097.1:c.384G= ENSP00000398776.1:p.Val128=
NM_000245.2:c.2544G= NP_000236.2:p.Val848=
NM_001127500.1:c.2598G= , LRG_662t1:c.2598G= NP_001120972.1:p.Val866=
XM_006715990.2:c.1254G= XP_006716053.1:p.Val418=
XM_006715991.2:c.1254G= XP_006716054.1:p.Val418=
XM_011516223.1:c.2601G= XP_011514525.1:p.Val867=
NM_000245.3:c.2544G= NP_000236.2:p.Val848=
NM_001127500.2:c.2598G= NP_001120972.1:p.Val866=
NM_001324401.1:c.2544G= NP_001311330.1:p.Val848=
NM_001324402.1:c.1254G= NP_001311331.1:p.Val418=
XR_001744772.1:n.2675G=
NM_001127500.3:c.2598G= NP_001120972.1:p.Val866=
NM_000245.4:c.2544G= MANE Select NP_000236.2:p.Val848=
NM_001324401.2:c.2544G= NP_001311330.1:p.Val848=
NM_001324402.2:c.1254G= NP_001311331.1:p.Val418=
NM_001324401.3:c.2544G= NP_001311330.1:p.Val848=