Canonical Allele Identifier: CA164909062

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116778816G>A , CM000669.2:g.116778816G>A	GRCh38
NC_000007.13:g.116418870G>A , CM000669.1:g.116418870G>A	GRCh37
NC_000007.12:g.116206106G>A	NCBI36
NG_008996.1:g.111412G>A , LRG_662:g.111412G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000245.4:c.3381G>A MANE Select	NP_000236.2:p.Glu1127=
ENST00000397752.8:c.3381G>A MANE Select	ENSP00000380860.3:p.Glu1127=
NM_000245.2:c.3381G>A	NP_000236.2:p.Glu1127=
NM_000245.3:c.3381G>A	NP_000236.2:p.Glu1127=
NM_001127500.1:c.3435G>A , LRG_662t1:c.3435G>A	NP_001120972.1:p.Glu1145=
NM_001127500.2:c.3435G>A	NP_001120972.1:p.Glu1145=
NM_001127500.3:c.3435G>A	NP_001120972.1:p.Glu1145=
NM_001324402.1:c.2091G>A	NP_001311331.1:p.Glu697=
NM_001324402.2:c.2091G>A	NP_001311331.1:p.Glu697=
ENST00000318493.10:c.3435G>A	ENSP00000317272.6:p.Glu1145=
ENST00000318493.11:c.3435G>A	ENSP00000317272.6:p.Glu1145=
ENST00000397752.7:c.3381G>A	ENSP00000380860.3:p.Glu1127=
ENST00000436117.3:c.*986G>A	ENSP00000410980.2:n.*986G>A
XM_006715990.2:c.2091G>A	XP_006716053.1:p.Glu697=
XM_006715991.2:c.2091G>A	XP_006716054.1:p.Glu697=
XM_011516223.1:c.3438G>A	XP_011514525.1:p.Glu1146=
XR_001744772.1:n.3512G>A