Canonical Allele Identifier: CA368986910

Gene: MET

Linked Data

• dbSNP Id: rs2116995820
• MyVariant Identifiers: chr7:g.116411904T>G (hg19) ; chr7:g.116771850T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771850T>G , CM000669.2:g.116771850T>G	GRCh38
NC_000007.13:g.116411904T>G , CM000669.1:g.116411904T>G	GRCh37
NC_000007.12:g.116199140T>G	NCBI36
NG_008996.1:g.104446T>G , LRG_662:g.104446T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*494T>G	ENSP00000410980.2:n.*494T>G
ENST00000318493.11:c.2943T>G	ENSP00000317272.6:p.Asp981Glu
ENST00000397752.8:c.2889T>G MANE Select	ENSP00000380860.3:p.Asp963Glu
ENST00000318493.10:c.2943T>G	ENSP00000317272.6:p.Asp981Glu
ENST00000397752.7:c.2889T>G	ENSP00000380860.3:p.Asp963Glu
ENST00000454623.1:c.283+196T>G	ENSP00000398140.1:n.283+196T>G
NM_000245.2:c.2889T>G	NP_000236.2:p.Asp963Glu
NM_001127500.1:c.2943T>G , LRG_662t1:c.2943T>G	NP_001120972.1:p.Asp981Glu
XM_006715990.2:c.1599T>G	XP_006716053.1:p.Asp533Glu
XM_006715991.2:c.1599T>G	XP_006716054.1:p.Asp533Glu
XM_011516223.1:c.2946T>G	XP_011514525.1:p.Asp982Glu
NM_000245.3:c.2889T>G	NP_000236.2:p.Asp963Glu
NM_001127500.2:c.2943T>G	NP_001120972.1:p.Asp981Glu
NM_001324402.1:c.1599T>G	NP_001311331.1:p.Asp533Glu
XR_001744772.1:n.3020T>G
NM_001127500.3:c.2943T>G	NP_001120972.1:p.Asp981Glu
NM_000245.4:c.2889T>G MANE Select	NP_000236.2:p.Asp963Glu
NM_001324402.2:c.1599T>G	NP_001311331.1:p.Asp533Glu