Canonical Allele Identifier: CA2740097508
Gene: MET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116757518_116757519delinsGC , CM000669.2:g.116757518_116757519delinsGC GRCh38
NC_000007.13:g.116397572_116397573delinsGC , CM000669.1:g.116397572_116397573delinsGC GRCh37
NC_000007.12:g.116184808_116184809delinsGC NCBI36
NG_008996.1:g.90114_90115delinsGC , LRG_662:g.90114_90115delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000422097.2:c.1944_1945delinsGC ENSP00000398776.2:p.Tyr649His
ENST00000436117.3:c.1944_1945delinsGC ENSP00000410980.2:p.Tyr649His
ENST00000318493.11:c.1944_1945delinsGC ENSP00000317272.6:p.Tyr649His
ENST00000397752.8:c.1944_1945delinsGC MANE Select ENSP00000380860.3:p.Tyr649His
ENST00000318493.10:c.1944_1945delinsGC ENSP00000317272.6:p.Tyr649His
ENST00000397752.7:c.1944_1945delinsGC ENSP00000380860.3:p.Tyr649His
ENST00000436117.2:c.1944_1945delinsGC ENSP00000410980.2:p.Tyr649His
NM_000245.2:c.1944_1945delinsGC NP_000236.2:p.Tyr649His
NM_001127500.1:c.1944_1945delinsGC , LRG_662t1:c.1944_1945delinsGC NP_001120972.1:p.Tyr649His
XM_006715990.2:c.654_655delinsGC XP_006716053.1:p.Tyr219His
XM_006715991.2:c.654_655delinsGC XP_006716054.1:p.Tyr219His
XM_011516223.1:c.2001_2002delinsGC XP_011514525.1:p.Tyr668His
NM_000245.3:c.1944_1945delinsGC NP_000236.2:p.Tyr649His
NM_001127500.2:c.1944_1945delinsGC NP_001120972.1:p.Tyr649His
NM_001324401.1:c.1944_1945delinsGC NP_001311330.1:p.Tyr649His
NM_001324402.1:c.654_655delinsGC NP_001311331.1:p.Tyr219His
XR_001744772.1:n.2175_2176delinsGC
NM_001127500.3:c.1944_1945delinsGC NP_001120972.1:p.Tyr649His
NM_000245.4:c.1944_1945delinsGC MANE Select NP_000236.2:p.Tyr649His
NM_001324401.2:c.1944_1945delinsGC NP_001311330.1:p.Tyr649His
NM_001324402.2:c.654_655delinsGC NP_001311331.1:p.Tyr219His
NM_001324401.3:c.1944_1945delinsGC NP_001311330.1:p.Tyr649His