Canonical Allele Identifier: CA1737029456
Gene: MET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116763116C= , CM000669.2:g.116763116C= GRCh38
NC_000007.13:g.116403170C= , CM000669.1:g.116403170C= GRCh37
NC_000007.12:g.116190406C= NCBI36
NG_008996.1:g.95712C= , LRG_662:g.95712C=

Transcript Alleles

HGVS Amino-acid change
ENST00000422097.2:c.2431C= ENSP00000398776.2:p.Leu811=
ENST00000436117.3:c.*36C= ENSP00000410980.2:n.*36C=
ENST00000318493.11:c.2485C= ENSP00000317272.6:p.Leu829=
ENST00000397752.8:c.2431C= MANE Select ENSP00000380860.3:p.Leu811=
ENST00000318493.10:c.2485C= ENSP00000317272.6:p.Leu829=
ENST00000397752.7:c.2431C= ENSP00000380860.3:p.Leu811=
ENST00000422097.1:c.271C= ENSP00000398776.1:p.Leu91=
NM_000245.2:c.2431C= NP_000236.2:p.Leu811=
NM_001127500.1:c.2485C= , LRG_662t1:c.2485C= NP_001120972.1:p.Leu829=
XM_006715990.2:c.1141C= XP_006716053.1:p.Leu381=
XM_006715991.2:c.1141C= XP_006716054.1:p.Leu381=
XM_011516223.1:c.2488C= XP_011514525.1:p.Leu830=
NM_000245.3:c.2431C= NP_000236.2:p.Leu811=
NM_001127500.2:c.2485C= NP_001120972.1:p.Leu829=
NM_001324401.1:c.2431C= NP_001311330.1:p.Leu811=
NM_001324402.1:c.1141C= NP_001311331.1:p.Leu381=
XR_001744772.1:n.2562C=
NM_001127500.3:c.2485C= NP_001120972.1:p.Leu829=
NM_000245.4:c.2431C= MANE Select NP_000236.2:p.Leu811=
NM_001324401.2:c.2431C= NP_001311330.1:p.Leu811=
NM_001324402.2:c.1141C= NP_001311331.1:p.Leu381=
NM_001324401.3:c.2431C= NP_001311330.1:p.Leu811=