Canonical Allele Identifier: CA2603544598

Gene: MET

Linked Data

• gnomAD v3: 7-116783162-G-GAGGCCAGATGAAATAGAGGCC
• gnomAD v4: 7-116783162-G-GAGGCCAGATGAAATAGAGGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783162_116783163insAGGCCAGATGAAATAGAGGCC , CM000669.2:g.116783162_116783163insAGGCCAGATGAAATAGAGGCC	GRCh38
NC_000007.13:g.116423216_116423217insAGGCCAGATGAAATAGAGGCC , CM000669.1:g.116423216_116423217insAGGCCAGATGAAATAGAGGCC	GRCh37
NC_000007.12:g.116210452_116210453insAGGCCAGATGAAATAGAGGCC	NCBI36
NG_008996.1:g.115758_115759insAGGCCAGATGAAATAGAGGCC , LRG_662:g.115758_115759insAGGCCAGATGAAATAGAGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*1238-142_*1238-141insAGGCCAGATGAAATAGAGGCC	ENSP00000410980.2:n.*1238-142_*1238-141insAGGCCAGATGAAATAGAGG...
ENST00000318493.11:c.3687-142_3687-141insAGGCCAGATGAAATAGAGGCC	ENSP00000317272.6:n.3687-142_3687-141insAGGCCAGATGAAATAGAGGCC...
ENST00000397752.8:c.3633-142_3633-141insAGGCCAGATGAAATAGAGGCC MANE Select	ENSP00000380860.3:n.3633-142_3633-141insAGGCCAGATGAAATAGAGGCC...
ENST00000318493.10:c.3687-142_3687-141insAGGCCAGATGAAATAGAGGCC	ENSP00000317272.6:n.3687-142_3687-141insAGGCCAGATGAAATAGAGGCC...
ENST00000397752.7:c.3633-142_3633-141insAGGCCAGATGAAATAGAGGCC	ENSP00000380860.3:n.3633-142_3633-141insAGGCCAGATGAAATAGAGGCC...
NM_000245.2:c.3633-142_3633-141insAGGCCAGATGAAATAGAGGCC	NP_000236.2:n.3633-142_3633-141insAGGCCAGATGAAATAGAGGCC
NM_001127500.1:c.3687-142_3687-141insAGGCCAGATGAAATAGAGGCC , LRG_662t1:c.3687-142_3687-141insAGGCCAGATGAAATAGAGGCC	NP_001120972.1:n.3687-142_3687-141insAGGCCAGATGAAATAGAGGCC
XM_006715990.2:c.2343-142_2343-141insAGGCCAGATGAAATAGAGGCC	XP_006716053.1:n.2343-142_2343-141insAGGCCAGATGAAATAGAGGCC
XM_006715991.2:c.2343-142_2343-141insAGGCCAGATGAAATAGAGGCC	XP_006716054.1:n.2343-142_2343-141insAGGCCAGATGAAATAGAGGCC
XM_011516223.1:c.3690-142_3690-141insAGGCCAGATGAAATAGAGGCC	XP_011514525.1:n.3690-142_3690-141insAGGCCAGATGAAATAGAGGCC
NM_000245.3:c.3633-142_3633-141insAGGCCAGATGAAATAGAGGCC	NP_000236.2:n.3633-142_3633-141insAGGCCAGATGAAATAGAGGCC
NM_001127500.2:c.3687-142_3687-141insAGGCCAGATGAAATAGAGGCC	NP_001120972.1:n.3687-142_3687-141insAGGCCAGATGAAATAGAGGCC
NM_001324402.1:c.2343-142_2343-141insAGGCCAGATGAAATAGAGGCC	NP_001311331.1:n.2343-142_2343-141insAGGCCAGATGAAATAGAGGCC
XR_001744772.1:n.3764-142_3764-141insAGGCCAGATGAAATAGAGGCC
NM_001127500.3:c.3687-142_3687-141insAGGCCAGATGAAATAGAGGCC	NP_001120972.1:n.3687-142_3687-141insAGGCCAGATGAAATAGAGGCC
NM_000245.4:c.3633-142_3633-141insAGGCCAGATGAAATAGAGGCC MANE Select	NP_000236.2:n.3633-142_3633-141insAGGCCAGATGAAATAGAGGCC
NM_001324402.2:c.2343-142_2343-141insAGGCCAGATGAAATAGAGGCC	NP_001311331.1:n.2343-142_2343-141insAGGCCAGATGAAATAGAGGCC