Canonical Allele Identifier: CA1737013966
Gene: MET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116783162G= , CM000669.2:g.116783162G= GRCh38
NC_000007.13:g.116423216G= , CM000669.1:g.116423216G= GRCh37
NC_000007.12:g.116210452G= NCBI36
NG_008996.1:g.115758G= , LRG_662:g.115758G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000436117.3:c.*1238-142G= ENSP00000410980.2:n.*1238-142G=
ENST00000318493.11:c.3687-142G= ENSP00000317272.6:n.3687-142G=
ENST00000397752.8:c.3633-142G= MANE Select ENSP00000380860.3:n.3633-142G=
ENST00000318493.10:c.3687-142G= ENSP00000317272.6:n.3687-142G=
ENST00000397752.7:c.3633-142G= ENSP00000380860.3:n.3633-142G=
NM_000245.2:c.3633-142G= NP_000236.2:n.3633-142G=
NM_001127500.1:c.3687-142G= , LRG_662t1:c.3687-142G= NP_001120972.1:n.3687-142G=
XM_006715990.2:c.2343-142G= XP_006716053.1:n.2343-142G=
XM_006715991.2:c.2343-142G= XP_006716054.1:n.2343-142G=
XM_011516223.1:c.3690-142G= XP_011514525.1:n.3690-142G=
NM_000245.3:c.3633-142G= NP_000236.2:n.3633-142G=
NM_001127500.2:c.3687-142G= NP_001120972.1:n.3687-142G=
NM_001324402.1:c.2343-142G= NP_001311331.1:n.2343-142G=
XR_001744772.1:n.3764-142G=
NM_001127500.3:c.3687-142G= NP_001120972.1:n.3687-142G=
NM_000245.4:c.3633-142G= MANE Select NP_000236.2:n.3633-142G=
NM_001324402.2:c.2343-142G= NP_001311331.1:n.2343-142G=