Canonical Allele Identifier: CA1737039889

Gene: MET

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_000245.4:c.3281A= MANE Select	NP_000236.2:p.His1094=
ENST00000397752.8:c.3281A= MANE Select	ENSP00000380860.3:p.His1094=
NM_000245.2:c.3281A=	NP_000236.2:p.His1094=
NM_000245.3:c.3281A=	NP_000236.2:p.His1094=
NM_001127500.1:c.3335A= , LRG_662t1:c.3335A=	NP_001120972.1:p.His1112=
NM_001127500.2:c.3335A=	NP_001120972.1:p.His1112=
NM_001127500.3:c.3335A=	NP_001120972.1:p.His1112=
NM_001324402.1:c.1991A=	NP_001311331.1:p.His664=
NM_001324402.2:c.1991A=	NP_001311331.1:p.His664=
ENST00000318493.10:c.3335A=	ENSP00000317272.6:p.His1112=
ENST00000318493.11:c.3335A=	ENSP00000317272.6:p.His1112=
ENST00000397752.7:c.3281A=	ENSP00000380860.3:p.His1094=
ENST00000436117.3:c.*886A=	ENSP00000410980.2:n.*886A=
XM_006715990.2:c.1991A=	XP_006716053.1:p.His664=
XM_006715991.2:c.1991A=	XP_006716054.1:p.His664=
XM_011516223.1:c.3338A=	XP_011514525.1:p.His1113=
XR_001744772.1:n.3412A=