Canonical Allele Identifier: CA2777570115
Gene: MET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116783189C>G , CM000669.2:g.116783189C>G GRCh38
NC_000007.13:g.116423243C>G , CM000669.1:g.116423243C>G GRCh37
NC_000007.12:g.116210479C>G NCBI36
NG_008996.1:g.115785C>G , LRG_662:g.115785C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000436117.3:c.*1238-115C>G ENSP00000410980.2:n.*1238-115C>G
ENST00000318493.11:c.3687-115C>G ENSP00000317272.6:n.3687-115C>G
ENST00000397752.8:c.3633-115C>G MANE Select ENSP00000380860.3:n.3633-115C>G
ENST00000318493.10:c.3687-115C>G ENSP00000317272.6:n.3687-115C>G
ENST00000397752.7:c.3633-115C>G ENSP00000380860.3:n.3633-115C>G
NM_000245.2:c.3633-115C>G NP_000236.2:n.3633-115C>G
NM_001127500.1:c.3687-115C>G , LRG_662t1:c.3687-115C>G NP_001120972.1:n.3687-115C>G
XM_006715990.2:c.2343-115C>G XP_006716053.1:n.2343-115C>G
XM_006715991.2:c.2343-115C>G XP_006716054.1:n.2343-115C>G
XM_011516223.1:c.3690-115C>G XP_011514525.1:n.3690-115C>G
NM_000245.3:c.3633-115C>G NP_000236.2:n.3633-115C>G
NM_001127500.2:c.3687-115C>G NP_001120972.1:n.3687-115C>G
NM_001324402.1:c.2343-115C>G NP_001311331.1:n.2343-115C>G
XR_001744772.1:n.3764-115C>G
NM_001127500.3:c.3687-115C>G NP_001120972.1:n.3687-115C>G
NM_000245.4:c.3633-115C>G MANE Select NP_000236.2:n.3633-115C>G
NM_001324402.2:c.2343-115C>G NP_001311331.1:n.2343-115C>G