Canonical Allele Identifier: CA1737037452

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771641A= , CM000669.2:g.116771641A=	GRCh38
NC_000007.13:g.116411695A= , CM000669.1:g.116411695A=	GRCh37
NC_000007.12:g.116198931A=	NCBI36
NG_008996.1:g.104237A= , LRG_662:g.104237A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*479A=	ENSP00000410980.2:n.*479A=
ENST00000318493.11:c.2928A=	ENSP00000317272.6:p.Arg976=
ENST00000397752.8:c.2874A= MANE Select	ENSP00000380860.3:p.Arg958=
ENST00000318493.10:c.2928A=	ENSP00000317272.6:p.Arg976=
ENST00000397752.7:c.2874A=	ENSP00000380860.3:p.Arg958=
ENST00000454623.1:c.270A=	ENSP00000398140.1:p.Arg90=
NM_000245.2:c.2874A=	NP_000236.2:p.Arg958=
NM_001127500.1:c.2928A= , LRG_662t1:c.2928A=	NP_001120972.1:p.Arg976=
XM_006715990.2:c.1584A=	XP_006716053.1:p.Arg528=
XM_006715991.2:c.1584A=	XP_006716054.1:p.Arg528=
XM_011516223.1:c.2931A=	XP_011514525.1:p.Arg977=
NM_000245.3:c.2874A=	NP_000236.2:p.Arg958=
NM_001127500.2:c.2928A=	NP_001120972.1:p.Arg976=
NM_001324402.1:c.1584A=	NP_001311331.1:p.Arg528=
XR_001744772.1:n.3005A=
NM_001127500.3:c.2928A=	NP_001120972.1:p.Arg976=
NM_000245.4:c.2874A= MANE Select	NP_000236.2:p.Arg958=
NM_001324402.2:c.1584A=	NP_001311331.1:p.Arg528=