Canonical Allele Identifier: CA4448792

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116795720C>T , CM000669.2:g.116795720C>T	GRCh38
NC_000007.13:g.116435774C>T , CM000669.1:g.116435774C>T	GRCh37
NC_000007.12:g.116223010C>T	NCBI36
NG_008996.1:g.128316C>T , LRG_662:g.128316C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000245.4:c.3864C>T MANE Select	NP_000236.2:p.Asn1288=
ENST00000397752.8:c.3864C>T MANE Select	ENSP00000380860.3:p.Asn1288=
NM_000245.2:c.3864C>T	NP_000236.2:p.Asn1288=
NM_000245.3:c.3864C>T	NP_000236.2:p.Asn1288=
NM_001127500.1:c.3918C>T , LRG_662t1:c.3918C>T	NP_001120972.1:p.Asn1306=
NM_001127500.2:c.3918C>T	NP_001120972.1:p.Asn1306=
NM_001127500.3:c.3918C>T	NP_001120972.1:p.Asn1306=
NM_001324402.1:c.2574C>T	NP_001311331.1:p.Asn858=
NM_001324402.2:c.2574C>T	NP_001311331.1:p.Asn858=
ENST00000318493.10:c.3918C>T	ENSP00000317272.6:p.Asn1306=
ENST00000318493.11:c.3918C>T	ENSP00000317272.6:p.Asn1306=
ENST00000397752.7:c.3864C>T	ENSP00000380860.3:p.Asn1288=
ENST00000436117.3:c.*1469C>T	ENSP00000410980.2:n.*1469C>T
XM_006715990.2:c.2574C>T	XP_006716053.1:p.Asn858=
XM_006715991.2:c.2574C>T	XP_006716054.1:p.Asn858=
XM_011516223.1:c.3921C>T	XP_011514525.1:p.Asn1307=
XR_001744772.1:n.3995C>T