Canonical Allele Identifier: CA918110679

Gene: MET

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783295_116783296insC , CM000669.2:g.116783295_116783296insC	GRCh38
NC_000007.13:g.116423349_116423350insC , CM000669.1:g.116423349_116423350insC	GRCh37
NC_000007.12:g.116210585_116210586insC	NCBI36
NG_008996.1:g.115891_115892insC , LRG_662:g.115891_115892insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*1238-9_*1238-8insC	ENSP00000410980.2:n.*1238-9_*1238-8insC
ENST00000318493.11:c.3687-9_3687-8insC	ENSP00000317272.6:n.3687-9_3687-8insC
ENST00000397752.8:c.3633-9_3633-8insC MANE Select	ENSP00000380860.3:n.3633-9_3633-8insC
ENST00000318493.10:c.3687-9_3687-8insC	ENSP00000317272.6:n.3687-9_3687-8insC
ENST00000397752.7:c.3633-9_3633-8insC	ENSP00000380860.3:n.3633-9_3633-8insC
NM_000245.2:c.3633-9_3633-8insC	NP_000236.2:n.3633-9_3633-8insC
NM_001127500.1:c.3687-9_3687-8insC , LRG_662t1:c.3687-9_3687-8insC	NP_001120972.1:n.3687-9_3687-8insC
XM_006715990.2:c.2343-9_2343-8insC	XP_006716053.1:n.2343-9_2343-8insC
XM_006715991.2:c.2343-9_2343-8insC	XP_006716054.1:n.2343-9_2343-8insC
XM_011516223.1:c.3690-9_3690-8insC	XP_011514525.1:n.3690-9_3690-8insC
NM_000245.3:c.3633-9_3633-8insC	NP_000236.2:n.3633-9_3633-8insC
NM_001127500.2:c.3687-9_3687-8insC	NP_001120972.1:n.3687-9_3687-8insC
NM_001324402.1:c.2343-9_2343-8insC	NP_001311331.1:n.2343-9_2343-8insC
XR_001744772.1:n.3764-9_3764-8insC
NM_001127500.3:c.3687-9_3687-8insC	NP_001120972.1:n.3687-9_3687-8insC
NM_000245.4:c.3633-9_3633-8insC MANE Select	NP_000236.2:n.3633-9_3633-8insC
NM_001324402.2:c.2343-9_2343-8insC	NP_001311331.1:n.2343-9_2343-8insC