Canonical Allele Identifier: CA368983159

Gene: MET

Linked Data

• dbSNP Id: rs1584946893
• MyVariant Identifiers: chr7:g.116403170C>G (hg19) ; chr7:g.116763116C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116763116C>G , CM000669.2:g.116763116C>G	GRCh38
NC_000007.13:g.116403170C>G , CM000669.1:g.116403170C>G	GRCh37
NC_000007.12:g.116190406C>G	NCBI36
NG_008996.1:g.95712C>G , LRG_662:g.95712C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000422097.2:c.2431C>G	ENSP00000398776.2:p.Leu811Val
ENST00000436117.3:c.*36C>G	ENSP00000410980.2:n.*36C>G
ENST00000318493.11:c.2485C>G	ENSP00000317272.6:p.Leu829Val
ENST00000397752.8:c.2431C>G MANE Select	ENSP00000380860.3:p.Leu811Val
ENST00000318493.10:c.2485C>G	ENSP00000317272.6:p.Leu829Val
ENST00000397752.7:c.2431C>G	ENSP00000380860.3:p.Leu811Val
ENST00000422097.1:c.271C>G	ENSP00000398776.1:p.Leu91Val
NM_000245.2:c.2431C>G	NP_000236.2:p.Leu811Val
NM_001127500.1:c.2485C>G , LRG_662t1:c.2485C>G	NP_001120972.1:p.Leu829Val
XM_006715990.2:c.1141C>G	XP_006716053.1:p.Leu381Val
XM_006715991.2:c.1141C>G	XP_006716054.1:p.Leu381Val
XM_011516223.1:c.2488C>G	XP_011514525.1:p.Leu830Val
NM_000245.3:c.2431C>G	NP_000236.2:p.Leu811Val
NM_001127500.2:c.2485C>G	NP_001120972.1:p.Leu829Val
NM_001324401.1:c.2431C>G	NP_001311330.1:p.Leu811Val
NM_001324402.1:c.1141C>G	NP_001311331.1:p.Leu381Val
XR_001744772.1:n.2562C>G
NM_001127500.3:c.2485C>G	NP_001120972.1:p.Leu829Val
NM_000245.4:c.2431C>G MANE Select	NP_000236.2:p.Leu811Val
NM_001324401.2:c.2431C>G	NP_001311330.1:p.Leu811Val
NM_001324402.2:c.1141C>G	NP_001311331.1:p.Leu381Val
NM_001324401.3:c.2431C>G	NP_001311330.1:p.Leu811Val