Canonical Allele Identifier: CA368974069

Gene: MET

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116739984A>G , CM000669.2:g.116739984A>G	GRCh38
NC_000007.13:g.116380038A>G , CM000669.1:g.116380038A>G	GRCh37
NC_000007.12:g.116167274A>G	NCBI36
NG_008996.1:g.72580A>G , LRG_662:g.72580A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.1427A>G	ENSP00000398776.2:p.His476Arg
ENST00000436117.3:c.1427A>G	ENSP00000410980.2:p.His476Arg
ENST00000318493.11:c.1427A>G	ENSP00000317272.6:p.His476Arg
ENST00000397752.8:c.1427A>G MANE Select	ENSP00000380860.3:p.His476Arg
ENST00000318493.10:c.1427A>G	ENSP00000317272.6:p.His476Arg
ENST00000397752.7:c.1427A>G	ENSP00000380860.3:p.His476Arg
ENST00000436117.2:c.1427A>G	ENSP00000410980.2:p.His476Arg
ENST00000495962.1:n.407A>G
NM_000245.2:c.1427A>G	NP_000236.2:p.His476Arg
NM_001127500.1:c.1427A>G , LRG_662t1:c.1427A>G	NP_001120972.1:p.His476Arg
XM_006715990.2:c.137A>G	XP_006716053.1:p.His46Arg
XM_006715991.2:c.137A>G	XP_006716054.1:p.His46Arg
XM_011516223.1:c.1484A>G	XP_011514525.1:p.His495Arg
NM_000245.3:c.1427A>G	NP_000236.2:p.His476Arg
NM_001127500.2:c.1427A>G	NP_001120972.1:p.His476Arg
NM_001324401.1:c.1427A>G	NP_001311330.1:p.His476Arg
NM_001324402.1:c.137A>G	NP_001311331.1:p.His46Arg
XR_001744772.1:n.1658A>G
NM_001127500.3:c.1427A>G	NP_001120972.1:p.His476Arg
NM_000245.4:c.1427A>G MANE Select	NP_000236.2:p.His476Arg
NM_001324401.2:c.1427A>G	NP_001311330.1:p.His476Arg
NM_001324402.2:c.137A>G	NP_001311331.1:p.His46Arg
NM_001324401.3:c.1427A>G	NP_001311330.1:p.His476Arg