Canonical Allele Identifier: CA368989599

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116777410A>T , CM000669.2:g.116777410A>T	GRCh38
NC_000007.13:g.116417464A>T , CM000669.1:g.116417464A>T	GRCh37
NC_000007.12:g.116204700A>T	NCBI36
NG_008996.1:g.110006A>T , LRG_662:g.110006A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000245.4:c.3281A>T MANE Select	NP_000236.2:p.His1094Leu
ENST00000397752.8:c.3281A>T MANE Select	ENSP00000380860.3:p.His1094Leu
NM_000245.2:c.3281A>T	NP_000236.2:p.His1094Leu
NM_000245.3:c.3281A>T	NP_000236.2:p.His1094Leu
NM_001127500.1:c.3335A>T , LRG_662t1:c.3335A>T	NP_001120972.1:p.His1112Leu
NM_001127500.2:c.3335A>T	NP_001120972.1:p.His1112Leu
NM_001127500.3:c.3335A>T	NP_001120972.1:p.His1112Leu
NM_001324402.1:c.1991A>T	NP_001311331.1:p.His664Leu
NM_001324402.2:c.1991A>T	NP_001311331.1:p.His664Leu
ENST00000318493.10:c.3335A>T	ENSP00000317272.6:p.His1112Leu
ENST00000318493.11:c.3335A>T	ENSP00000317272.6:p.His1112Leu
ENST00000397752.7:c.3281A>T	ENSP00000380860.3:p.His1094Leu
ENST00000436117.3:c.*886A>T	ENSP00000410980.2:n.*886A>T
XM_006715990.2:c.1991A>T	XP_006716053.1:p.His664Leu
XM_006715991.2:c.1991A>T	XP_006716054.1:p.His664Leu
XM_011516223.1:c.3338A>T	XP_011514525.1:p.His1113Leu
XR_001744772.1:n.3412A>T