Canonical Allele Identifier: CA1737014020
Gene: MET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116783187_116783188delinsTC , CM000669.2:g.116783187_116783188delinsTC GRCh38
NC_000007.13:g.116423241_116423242delinsTC , CM000669.1:g.116423241_116423242delinsTC GRCh37
NC_000007.12:g.116210477_116210478delinsTC NCBI36
NG_008996.1:g.115783_115784delinsTC , LRG_662:g.115783_115784delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000436117.3:c.*1238-117_*1238-116delinsTC ENSP00000410980.2:n.*1238-117_*1238-116delinsTC
ENST00000318493.11:c.3687-117_3687-116delinsTC ENSP00000317272.6:n.3687-117_3687-116delinsTC
ENST00000397752.8:c.3633-117_3633-116delinsTC MANE Select ENSP00000380860.3:n.3633-117_3633-116delinsTC
ENST00000318493.10:c.3687-117_3687-116delinsTC ENSP00000317272.6:n.3687-117_3687-116delinsTC
ENST00000397752.7:c.3633-117_3633-116delinsTC ENSP00000380860.3:n.3633-117_3633-116delinsTC
NM_000245.2:c.3633-117_3633-116delinsTC NP_000236.2:n.3633-117_3633-116delinsTC
NM_001127500.1:c.3687-117_3687-116delinsTC , LRG_662t1:c.3687-117_3687-116delinsTC NP_001120972.1:n.3687-117_3687-116delinsTC
XM_006715990.2:c.2343-117_2343-116delinsTC XP_006716053.1:n.2343-117_2343-116delinsTC
XM_006715991.2:c.2343-117_2343-116delinsTC XP_006716054.1:n.2343-117_2343-116delinsTC
XM_011516223.1:c.3690-117_3690-116delinsTC XP_011514525.1:n.3690-117_3690-116delinsTC
NM_000245.3:c.3633-117_3633-116delinsTC NP_000236.2:n.3633-117_3633-116delinsTC
NM_001127500.2:c.3687-117_3687-116delinsTC NP_001120972.1:n.3687-117_3687-116delinsTC
NM_001324402.1:c.2343-117_2343-116delinsTC NP_001311331.1:n.2343-117_2343-116delinsTC
XR_001744772.1:n.3764-117_3764-116delinsTC
NM_001127500.3:c.3687-117_3687-116delinsTC NP_001120972.1:n.3687-117_3687-116delinsTC
NM_000245.4:c.3633-117_3633-116delinsTC MANE Select NP_000236.2:n.3633-117_3633-116delinsTC
NM_001324402.2:c.2343-117_2343-116delinsTC NP_001311331.1:n.2343-117_2343-116delinsTC