Canonical Allele Identifier: CA349710

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116796096G>A , CM000669.2:g.116796096G>A	GRCh38
NC_000007.13:g.116436150G>A , CM000669.1:g.116436150G>A	GRCh37
NC_000007.12:g.116223386G>A	NCBI36
NG_008996.1:g.128692G>A , LRG_662:g.128692G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000245.4:c.4145G>A MANE Select	NP_000236.2:p.Arg1382Gln
ENST00000397752.8:c.4145G>A MANE Select	ENSP00000380860.3:p.Arg1382Gln
NM_000245.2:c.4145G>A	NP_000236.2:p.Arg1382Gln
NM_000245.3:c.4145G>A	NP_000236.2:p.Arg1382Gln
NM_001127500.1:c.4199G>A , LRG_662t1:c.4199G>A	NP_001120972.1:p.Arg1400Gln
NM_001127500.2:c.4199G>A	NP_001120972.1:p.Arg1400Gln
NM_001127500.3:c.4199G>A	NP_001120972.1:p.Arg1400Gln
NM_001324402.1:c.2855G>A	NP_001311331.1:p.Arg952Gln
NM_001324402.2:c.2855G>A	NP_001311331.1:p.Arg952Gln
ENST00000318493.10:c.4199G>A	ENSP00000317272.6:p.Arg1400Gln
ENST00000318493.11:c.4199G>A	ENSP00000317272.6:p.Arg1400Gln
ENST00000397752.7:c.4145G>A	ENSP00000380860.3:p.Arg1382Gln
ENST00000436117.3:c.*1750G>A	ENSP00000410980.2:n.*1750G>A
XM_006715990.2:c.2855G>A	XP_006716053.1:p.Arg952Gln
XM_006715991.2:c.2855G>A	XP_006716054.1:p.Arg952Gln
XM_011516223.1:c.4202G>A	XP_011514525.1:p.Arg1401Gln
XR_001744772.1:n.4276G>A