Canonical Allele Identifier: CA368991755

Gene: MET

Linked Data

• dbSNP Id: rs1166652916
• MyVariant Identifiers: chr7:g.116423447C>G (hg19) ; chr7:g.116783393C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783393C>G , CM000669.2:g.116783393C>G	GRCh38
NC_000007.13:g.116423447C>G , CM000669.1:g.116423447C>G	GRCh37
NC_000007.12:g.116210683C>G	NCBI36
NG_008996.1:g.115989C>G , LRG_662:g.115989C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*1327C>G	ENSP00000410980.2:n.*1327C>G
ENST00000318493.11:c.3776C>G	ENSP00000317272.6:p.Thr1259Arg
ENST00000397752.8:c.3722C>G MANE Select	ENSP00000380860.3:p.Thr1241Arg
ENST00000318493.10:c.3776C>G	ENSP00000317272.6:p.Thr1259Arg
ENST00000397752.7:c.3722C>G	ENSP00000380860.3:p.Thr1241Arg
NM_000245.2:c.3722C>G	NP_000236.2:p.Thr1241Arg
NM_001127500.1:c.3776C>G , LRG_662t1:c.3776C>G	NP_001120972.1:p.Thr1259Arg
XM_006715990.2:c.2432C>G	XP_006716053.1:p.Thr811Arg
XM_006715991.2:c.2432C>G	XP_006716054.1:p.Thr811Arg
XM_011516223.1:c.3779C>G	XP_011514525.1:p.Thr1260Arg
NM_000245.3:c.3722C>G	NP_000236.2:p.Thr1241Arg
NM_001127500.2:c.3776C>G	NP_001120972.1:p.Thr1259Arg
NM_001324402.1:c.2432C>G	NP_001311331.1:p.Thr811Arg
XR_001744772.1:n.3853C>G
NM_001127500.3:c.3776C>G	NP_001120972.1:p.Thr1259Arg
NM_000245.4:c.3722C>G MANE Select	NP_000236.2:p.Thr1241Arg
NM_001324402.2:c.2432C>G	NP_001311331.1:p.Thr811Arg