Canonical Allele Identifier: CA1737031127

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116796211G= , CM000669.2:g.116796211G=	GRCh38
NC_000007.13:g.116436265G= , CM000669.1:g.116436265G=	GRCh37
NC_000007.12:g.116223501G=	NCBI36
NG_008996.1:g.128807G= , LRG_662:g.128807G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*1865G=	ENSP00000410980.2:n.*1865G=
ENST00000318493.11:c.*87G=	ENSP00000317272.6:n.*87G=
ENST00000397752.8:c.*87G= MANE Select	ENSP00000380860.3:n.*87G=
ENST00000318493.10:c.*87G=	ENSP00000317272.6:n.*87G=
ENST00000397752.7:c.*87G=	ENSP00000380860.3:n.*87G=
NM_000245.2:c.*87G=	NP_000236.2:n.*87G=
NM_001127500.1:c.*87G= , LRG_662t1:c.*87G=	NP_001120972.1:n.*87G=
XM_006715990.2:c.*87G=	XP_006716053.1:n.*87G=
XM_006715991.2:c.*87G=	XP_006716054.1:n.*87G=
XM_011516223.1:c.*87G=	XP_011514525.1:n.*87G=
NM_000245.3:c.*87G=	NP_000236.2:n.*87G=
NM_001127500.2:c.*87G=	NP_001120972.1:n.*87G=
NM_001324402.1:c.*87G=	NP_001311331.1:n.*87G=
XR_001744772.1:n.4391G=
NM_001127500.3:c.*87G=	NP_001120972.1:n.*87G=
NM_000245.4:c.*87G= MANE Select	NP_000236.2:n.*87G=
NM_001324402.2:c.*87G=	NP_001311331.1:n.*87G=