Canonical Allele Identifier: CA457447573

Gene: MET

Linked Data

• dbSNP Id: rs2116996815
• MyVariant Identifiers: chr7:g.116411976A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771922A>T , CM000669.2:g.116771922A>T	GRCh38
NC_000007.13:g.116411976A>T , CM000669.1:g.116411976A>T	GRCh37
NC_000007.12:g.116199212A>T	NCBI36
NG_008996.1:g.104518A>T , LRG_662:g.104518A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*566A>T	ENSP00000410980.2:n.*566A>T
ENST00000318493.11:c.3015A>T	ENSP00000317272.6:p.Arg1005=
ENST00000397752.8:c.2961A>T MANE Select	ENSP00000380860.3:p.Arg987=
ENST00000318493.10:c.3015A>T	ENSP00000317272.6:p.Arg1005=
ENST00000397752.7:c.2961A>T	ENSP00000380860.3:p.Arg987=
ENST00000454623.1:c.283+268A>T	ENSP00000398140.1:n.283+268A>T
NM_000245.2:c.2961A>T	NP_000236.2:p.Arg987=
NM_001127500.1:c.3015A>T , LRG_662t1:c.3015A>T	NP_001120972.1:p.Arg1005=
XM_006715990.2:c.1671A>T	XP_006716053.1:p.Arg557=
XM_006715991.2:c.1671A>T	XP_006716054.1:p.Arg557=
XM_011516223.1:c.3018A>T	XP_011514525.1:p.Arg1006=
NM_000245.3:c.2961A>T	NP_000236.2:p.Arg987=
NM_001127500.2:c.3015A>T	NP_001120972.1:p.Arg1005=
NM_001324402.1:c.1671A>T	NP_001311331.1:p.Arg557=
XR_001744772.1:n.3092A>T
NM_001127500.3:c.3015A>T	NP_001120972.1:p.Arg1005=
NM_000245.4:c.2961A>T MANE Select	NP_000236.2:p.Arg987=
NM_001324402.2:c.1671A>T	NP_001311331.1:p.Arg557=