Canonical Allele Identifier: CA1737037601

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771928A= , CM000669.2:g.116771928A=	GRCh38
NC_000007.13:g.116411982A= , CM000669.1:g.116411982A=	GRCh37
NC_000007.12:g.116199218A=	NCBI36
NG_008996.1:g.104524A= , LRG_662:g.104524A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*572A=	ENSP00000410980.2:n.*572A=
ENST00000318493.11:c.3021A=	ENSP00000317272.6:p.Val1007=
ENST00000397752.8:c.2967A= MANE Select	ENSP00000380860.3:p.Val989=
ENST00000318493.10:c.3021A=	ENSP00000317272.6:p.Val1007=
ENST00000397752.7:c.2967A=	ENSP00000380860.3:p.Val989=
ENST00000454623.1:c.283+274A=	ENSP00000398140.1:n.283+274A=
NM_000245.2:c.2967A=	NP_000236.2:p.Val989=
NM_001127500.1:c.3021A= , LRG_662t1:c.3021A=	NP_001120972.1:p.Val1007=
XM_006715990.2:c.1677A=	XP_006716053.1:p.Val559=
XM_006715991.2:c.1677A=	XP_006716054.1:p.Val559=
XM_011516223.1:c.3024A=	XP_011514525.1:p.Val1008=
NM_000245.3:c.2967A=	NP_000236.2:p.Val989=
NM_001127500.2:c.3021A=	NP_001120972.1:p.Val1007=
NM_001324402.1:c.1677A=	NP_001311331.1:p.Val559=
XR_001744772.1:n.3098A=
NM_001127500.3:c.3021A=	NP_001120972.1:p.Val1007=
NM_000245.4:c.2967A= MANE Select	NP_000236.2:p.Val989=
NM_001324402.2:c.1677A=	NP_001311331.1:p.Val559=