Canonical Allele Identifier: CA368991891

Gene: MET

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783420T>G , CM000669.2:g.116783420T>G	GRCh38
NC_000007.13:g.116423474T>G , CM000669.1:g.116423474T>G	GRCh37
NC_000007.12:g.116210710T>G	NCBI36
NG_008996.1:g.116016T>G , LRG_662:g.116016T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*1354T>G	ENSP00000410980.2:n.*1354T>G
ENST00000318493.11:c.3803T>G	ENSP00000317272.6:p.Met1268Arg
ENST00000397752.8:c.3749T>G MANE Select	ENSP00000380860.3:p.Met1250Arg
ENST00000318493.10:c.3803T>G	ENSP00000317272.6:p.Met1268Arg
ENST00000397752.7:c.3749T>G	ENSP00000380860.3:p.Met1250Arg
NM_000245.2:c.3749T>G	NP_000236.2:p.Met1250Arg
NM_001127500.1:c.3803T>G , LRG_662t1:c.3803T>G	NP_001120972.1:p.Met1268Arg
XM_006715990.2:c.2459T>G	XP_006716053.1:p.Met820Arg
XM_006715991.2:c.2459T>G	XP_006716054.1:p.Met820Arg
XM_011516223.1:c.3806T>G	XP_011514525.1:p.Met1269Arg
NM_000245.3:c.3749T>G	NP_000236.2:p.Met1250Arg
NM_001127500.2:c.3803T>G	NP_001120972.1:p.Met1268Arg
NM_001324402.1:c.2459T>G	NP_001311331.1:p.Met820Arg
XR_001744772.1:n.3880T>G
NM_001127500.3:c.3803T>G	NP_001120972.1:p.Met1268Arg
NM_000245.4:c.3749T>G MANE Select	NP_000236.2:p.Met1250Arg
NM_001324402.2:c.2459T>G	NP_001311331.1:p.Met820Arg