Canonical Allele Identifier: CA1737013964
Gene: MET HGNC NCBI

Linked Data

dbSNP Id: rs1795203184

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116783161_116783162insCAATAGAGGCCAGATGAAATAGAGGC , CM000669.2:g.116783161_116783162insCAATAGAGGCCAGATGAAATAGAGGC GRCh38
NC_000007.13:g.116423215_116423216insCAATAGAGGCCAGATGAAATAGAGGC , CM000669.1:g.116423215_116423216insCAATAGAGGCCAGATGAAATAGAGGC GRCh37
NC_000007.12:g.116210451_116210452insCAATAGAGGCCAGATGAAATAGAGGC NCBI36
NG_008996.1:g.115757_115758insCAATAGAGGCCAGATGAAATAGAGGC , LRG_662:g.115757_115758insCAATAGAGGCCAGATGAAATAGAGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000436117.3:c.*1238-143_*1238-142insCAATAGAGGCCAGATGAAATAGAGGC ENSP00000410980.2:n.*1238-143_*1238-142insCAATAGAGGCCAGATGAAA...
ENST00000318493.11:c.3687-143_3687-142insCAATAGAGGCCAGATGAAATAGAGGC ENSP00000317272.6:n.3687-143_3687-142insCAATAGAGGCCAGATGAAATA...
ENST00000397752.8:c.3633-143_3633-142insCAATAGAGGCCAGATGAAATAGAGGC MANE Select ENSP00000380860.3:n.3633-143_3633-142insCAATAGAGGCCAGATGAAATA...
ENST00000318493.10:c.3687-143_3687-142insCAATAGAGGCCAGATGAAATAGAGGC ENSP00000317272.6:n.3687-143_3687-142insCAATAGAGGCCAGATGAAATA...
ENST00000397752.7:c.3633-143_3633-142insCAATAGAGGCCAGATGAAATAGAGGC ENSP00000380860.3:n.3633-143_3633-142insCAATAGAGGCCAGATGAAATA...
NM_000245.2:c.3633-143_3633-142insCAATAGAGGCCAGATGAAATAGAGGC NP_000236.2:n.3633-143_3633-142insCAATAGAGGCCAGATGAAATAGAGGC
NM_001127500.1:c.3687-143_3687-142insCAATAGAGGCCAGATGAAATAGAGGC , LRG_662t1:c.3687-143_3687-142insCAATAGAGGCCAGATGAAATAGAGGC NP_001120972.1:n.3687-143_3687-142insCAATAGAGGCCAGATGAAATAGAG...
XM_006715990.2:c.2343-143_2343-142insCAATAGAGGCCAGATGAAATAGAGGC XP_006716053.1:n.2343-143_2343-142insCAATAGAGGCCAGATGAAATAGAG...
XM_006715991.2:c.2343-143_2343-142insCAATAGAGGCCAGATGAAATAGAGGC XP_006716054.1:n.2343-143_2343-142insCAATAGAGGCCAGATGAAATAGAG...
XM_011516223.1:c.3690-143_3690-142insCAATAGAGGCCAGATGAAATAGAGGC XP_011514525.1:n.3690-143_3690-142insCAATAGAGGCCAGATGAAATAGAG...
NM_000245.3:c.3633-143_3633-142insCAATAGAGGCCAGATGAAATAGAGGC NP_000236.2:n.3633-143_3633-142insCAATAGAGGCCAGATGAAATAGAGGC
NM_001127500.2:c.3687-143_3687-142insCAATAGAGGCCAGATGAAATAGAGGC NP_001120972.1:n.3687-143_3687-142insCAATAGAGGCCAGATGAAATAGAG...
NM_001324402.1:c.2343-143_2343-142insCAATAGAGGCCAGATGAAATAGAGGC NP_001311331.1:n.2343-143_2343-142insCAATAGAGGCCAGATGAAATAGAG...
XR_001744772.1:n.3764-143_3764-142insCAATAGAGGCCAGATGAAATAGAGGC
NM_001127500.3:c.3687-143_3687-142insCAATAGAGGCCAGATGAAATAGAGGC NP_001120972.1:n.3687-143_3687-142insCAATAGAGGCCAGATGAAATAGAG...
NM_000245.4:c.3633-143_3633-142insCAATAGAGGCCAGATGAAATAGAGGC MANE Select NP_000236.2:n.3633-143_3633-142insCAATAGAGGCCAGATGAAATAGAGGC
NM_001324402.2:c.2343-143_2343-142insCAATAGAGGCCAGATGAAATAGAGGC NP_001311331.1:n.2343-143_2343-142insCAATAGAGGCCAGATGAAATAGAG...