Canonical Allele Identifier: CA1737014402

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783363A= , CM000669.2:g.116783363A=	GRCh38
NC_000007.13:g.116423417A= , CM000669.1:g.116423417A=	GRCh37
NC_000007.12:g.116210653A=	NCBI36
NG_008996.1:g.115959A= , LRG_662:g.115959A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000436117.3:c.*1297A=	ENSP00000410980.2:n.*1297A=
ENST00000318493.11:c.3746A=	ENSP00000317272.6:p.Asp1249=
ENST00000397752.8:c.3692A= MANE Select	ENSP00000380860.3:p.Asp1231=
ENST00000318493.10:c.3746A=	ENSP00000317272.6:p.Asp1249=
ENST00000397752.7:c.3692A=	ENSP00000380860.3:p.Asp1231=
NM_000245.2:c.3692A=	NP_000236.2:p.Asp1231=
NM_001127500.1:c.3746A= , LRG_662t1:c.3746A=	NP_001120972.1:p.Asp1249=
XM_006715990.2:c.2402A=	XP_006716053.1:p.Asp801=
XM_006715991.2:c.2402A=	XP_006716054.1:p.Asp801=
XM_011516223.1:c.3749A=	XP_011514525.1:p.Asp1250=
NM_000245.3:c.3692A=	NP_000236.2:p.Asp1231=
NM_001127500.2:c.3746A=	NP_001120972.1:p.Asp1249=
NM_001324402.1:c.2402A=	NP_001311331.1:p.Asp801=
XR_001744772.1:n.3823A=
NM_001127500.3:c.3746A=	NP_001120972.1:p.Asp1249=
NM_000245.4:c.3692A= MANE Select	NP_000236.2:p.Asp1231=
NM_001324402.2:c.2402A=	NP_001311331.1:p.Asp801=