Canonical Allele Identifier: CA3054204815
Gene: MET HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116783296delinsCC , CM000669.2:g.116783296delinsCC GRCh38
NC_000007.13:g.116423350delinsCC , CM000669.1:g.116423350delinsCC GRCh37
NC_000007.12:g.116210586delinsCC NCBI36
NG_008996.1:g.115892delinsCC , LRG_662:g.115892delinsCC

Transcript Alleles

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