Canonical Allele Identifier: CA2684592621
Gene: MET HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116783215_116783220del , CM000669.2:g.116783215_116783220del GRCh38
NC_000007.13:g.116423269_116423274del , CM000669.1:g.116423269_116423274del GRCh37
NC_000007.12:g.116210505_116210510del NCBI36
NG_008996.1:g.115811_115816del , LRG_662:g.115811_115816del

Transcript Alleles

HGVS Amino-acid Change
ENST00000436117.3:c.*1238-89_*1238-84del ENSP00000410980.2:n.*1238-89_*1238-84del
ENST00000318493.11:c.3687-89_3687-84del ENSP00000317272.6:n.3687-89_3687-84del
ENST00000397752.8:c.3633-89_3633-84del MANE Select ENSP00000380860.3:n.3633-89_3633-84del
ENST00000318493.10:c.3687-89_3687-84del ENSP00000317272.6:n.3687-89_3687-84del
ENST00000397752.7:c.3633-89_3633-84del ENSP00000380860.3:n.3633-89_3633-84del
NM_000245.2:c.3633-89_3633-84del NP_000236.2:n.3633-89_3633-84del
NM_001127500.1:c.3687-89_3687-84del , LRG_662t1:c.3687-89_3687-84del NP_001120972.1:n.3687-89_3687-84del
XM_006715990.2:c.2343-89_2343-84del XP_006716053.1:n.2343-89_2343-84del
XM_006715991.2:c.2343-89_2343-84del XP_006716054.1:n.2343-89_2343-84del
XM_011516223.1:c.3690-89_3690-84del XP_011514525.1:n.3690-89_3690-84del
NM_000245.3:c.3633-89_3633-84del NP_000236.2:n.3633-89_3633-84del
NM_001127500.2:c.3687-89_3687-84del NP_001120972.1:n.3687-89_3687-84del
NM_001324402.1:c.2343-89_2343-84del NP_001311331.1:n.2343-89_2343-84del
XR_001744772.1:n.3764-89_3764-84del
NM_001127500.3:c.3687-89_3687-84del NP_001120972.1:n.3687-89_3687-84del
NM_000245.4:c.3633-89_3633-84del MANE Select NP_000236.2:n.3633-89_3633-84del
NM_001324402.2:c.2343-89_2343-84del NP_001311331.1:n.2343-89_2343-84del