Canonical Allele Identifier: CA4448584

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771522G>A , CM000669.2:g.116771522G>A	GRCh38
NC_000007.13:g.116411576G>A , CM000669.1:g.116411576G>A	GRCh37
NC_000007.12:g.116198812G>A	NCBI36
NG_008996.1:g.104118G>A , LRG_662:g.104118G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*360G>A	ENSP00000410980.2:n.*360G>A
ENST00000318493.11:c.2809G>A	ENSP00000317272.6:p.Val937Ile
ENST00000397752.8:c.2755G>A MANE Select	ENSP00000380860.3:p.Val919Ile
ENST00000318493.10:c.2809G>A	ENSP00000317272.6:p.Val937Ile
ENST00000397752.7:c.2755G>A	ENSP00000380860.3:p.Val919Ile
ENST00000454623.1:c.151G>A	ENSP00000398140.1:p.Val51Ile
NM_000245.2:c.2755G>A	NP_000236.2:p.Val919Ile
NM_001127500.1:c.2809G>A , LRG_662t1:c.2809G>A	NP_001120972.1:p.Val937Ile
XM_006715990.2:c.1465G>A	XP_006716053.1:p.Val489Ile
XM_006715991.2:c.1465G>A	XP_006716054.1:p.Val489Ile
XM_011516223.1:c.2812G>A	XP_011514525.1:p.Val938Ile
NM_000245.3:c.2755G>A	NP_000236.2:p.Val919Ile
NM_001127500.2:c.2809G>A	NP_001120972.1:p.Val937Ile
NM_001324402.1:c.1465G>A	NP_001311331.1:p.Val489Ile
XR_001744772.1:n.2886G>A
NM_001127500.3:c.2809G>A	NP_001120972.1:p.Val937Ile
NM_000245.4:c.2755G>A MANE Select	NP_000236.2:p.Val919Ile
NM_001324402.2:c.1465G>A	NP_001311331.1:p.Val489Ile