Canonical Allele Identifier: CA1737037620

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771971C= , CM000669.2:g.116771971C=	GRCh38
NC_000007.13:g.116412025C= , CM000669.1:g.116412025C=	GRCh37
NC_000007.12:g.116199261C=	NCBI36
NG_008996.1:g.104567C= , LRG_662:g.104567C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*615C=	ENSP00000410980.2:n.*615C=
ENST00000318493.11:c.3064C=	ENSP00000317272.6:p.Arg1022=
ENST00000397752.8:c.3010C= MANE Select	ENSP00000380860.3:p.Arg1004=
ENST00000318493.10:c.3064C=	ENSP00000317272.6:p.Arg1022=
ENST00000397752.7:c.3010C=	ENSP00000380860.3:p.Arg1004=
ENST00000454623.1:c.283+317C=	ENSP00000398140.1:n.283+317C=
NM_000245.2:c.3010C=	NP_000236.2:p.Arg1004=
NM_001127500.1:c.3064C= , LRG_662t1:c.3064C=	NP_001120972.1:p.Arg1022=
XM_006715990.2:c.1720C=	XP_006716053.1:p.Arg574=
XM_006715991.2:c.1720C=	XP_006716054.1:p.Arg574=
XM_011516223.1:c.3067C=	XP_011514525.1:p.Arg1023=
NM_000245.3:c.3010C=	NP_000236.2:p.Arg1004=
NM_001127500.2:c.3064C=	NP_001120972.1:p.Arg1022=
NM_001324402.1:c.1720C=	NP_001311331.1:p.Arg574=
XR_001744772.1:n.3141C=
NM_001127500.3:c.3064C=	NP_001120972.1:p.Arg1022=
NM_000245.4:c.3010C= MANE Select	NP_000236.2:p.Arg1004=
NM_001324402.2:c.1720C=	NP_001311331.1:p.Arg574=