Canonical Allele Identifier: CA457217227

Gene: MET

Linked Data

• dbSNP Id: rs2116937959
• MyVariant Identifiers: chr7:g.116399472G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759418G>A , CM000669.2:g.116759418G>A	GRCh38
NC_000007.13:g.116399472G>A , CM000669.1:g.116399472G>A	GRCh37
NC_000007.12:g.116186708G>A	NCBI36
NG_008996.1:g.92014G>A , LRG_662:g.92014G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2292G>A	ENSP00000398776.2:p.Gly764=
ENST00000436117.3:c.2264+798G>A	ENSP00000410980.2:n.2264+798G>A
ENST00000318493.11:c.2346G>A	ENSP00000317272.6:p.Gly782=
ENST00000397752.8:c.2292G>A MANE Select	ENSP00000380860.3:p.Gly764=
ENST00000318493.10:c.2346G>A	ENSP00000317272.6:p.Gly782=
ENST00000397752.7:c.2292G>A	ENSP00000380860.3:p.Gly764=
ENST00000422097.1:c.132G>A	ENSP00000398776.1:p.Gly44=
ENST00000436117.2:c.2264+798G>A	ENSP00000410980.2:n.2264+798G>A
NM_000245.2:c.2292G>A	NP_000236.2:p.Gly764=
NM_001127500.1:c.2346G>A , LRG_662t1:c.2346G>A	NP_001120972.1:p.Gly782=
XM_006715990.2:c.1002G>A	XP_006716053.1:p.Gly334=
XM_006715991.2:c.1002G>A	XP_006716054.1:p.Gly334=
XM_011516223.1:c.2349G>A	XP_011514525.1:p.Gly783=
NM_000245.3:c.2292G>A	NP_000236.2:p.Gly764=
NM_001127500.2:c.2346G>A	NP_001120972.1:p.Gly782=
NM_001324401.1:c.2292G>A	NP_001311330.1:p.Gly764=
NM_001324402.1:c.1002G>A	NP_001311331.1:p.Gly334=
XR_001744772.1:n.2495+798G>A
NM_001127500.3:c.2346G>A	NP_001120972.1:p.Gly782=
NM_000245.4:c.2292G>A MANE Select	NP_000236.2:p.Gly764=
NM_001324401.2:c.2292G>A	NP_001311330.1:p.Gly764=
NM_001324402.2:c.1002G>A	NP_001311331.1:p.Gly334=
NM_001324401.3:c.2292G>A	NP_001311330.1:p.Gly764=