Canonical Allele Identifier: CA4448648

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116774943A>G , CM000669.2:g.116774943A>G	GRCh38
NC_000007.13:g.116414997A>G , CM000669.1:g.116414997A>G	GRCh37
NC_000007.12:g.116202233A>G	NCBI36
NG_008996.1:g.107539A>G , LRG_662:g.107539A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000245.4:c.3091A>G MANE Select	NP_000236.2:p.Met1031Val
ENST00000397752.8:c.3091A>G MANE Select	ENSP00000380860.3:p.Met1031Val
NM_000245.2:c.3091A>G	NP_000236.2:p.Met1031Val
NM_000245.3:c.3091A>G	NP_000236.2:p.Met1031Val
NM_001127500.1:c.3145A>G , LRG_662t1:c.3145A>G	NP_001120972.1:p.Met1049Val
NM_001127500.2:c.3145A>G	NP_001120972.1:p.Met1049Val
NM_001127500.3:c.3145A>G	NP_001120972.1:p.Met1049Val
NM_001324402.1:c.1801A>G	NP_001311331.1:p.Met601Val
NM_001324402.2:c.1801A>G	NP_001311331.1:p.Met601Val
ENST00000318493.10:c.3145A>G	ENSP00000317272.6:p.Met1049Val
ENST00000318493.11:c.3145A>G	ENSP00000317272.6:p.Met1049Val
ENST00000397752.7:c.3091A>G	ENSP00000380860.3:p.Met1031Val
ENST00000436117.3:c.*696A>G	ENSP00000410980.2:n.*696A>G
ENST00000454623.1:c.346A>G	ENSP00000398140.1:p.Met116Val
XM_006715990.2:c.1801A>G	XP_006716053.1:p.Met601Val
XM_006715991.2:c.1801A>G	XP_006716054.1:p.Met601Val
XM_011516223.1:c.3148A>G	XP_011514525.1:p.Met1050Val
XR_001744772.1:n.3222A>G