Canonical Allele Identifier: CA4448031

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116699887C>T , CM000669.2:g.116699887C>T	GRCh38
NC_000007.13:g.116339941C>T , CM000669.1:g.116339941C>T	GRCh37
NC_000007.12:g.116127177C>T	NCBI36
NG_008996.1:g.32483C>T , LRG_662:g.32483C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.803C>T	ENSP00000398776.2:p.Thr268Ile
ENST00000436117.3:c.803C>T	ENSP00000410980.2:p.Thr268Ile
ENST00000318493.11:c.803C>T	ENSP00000317272.6:p.Thr268Ile
ENST00000397752.8:c.803C>T MANE Select	ENSP00000380860.3:p.Thr268Ile
ENST00000318493.10:c.803C>T	ENSP00000317272.6:p.Thr268Ile
ENST00000397752.7:c.803C>T	ENSP00000380860.3:p.Thr268Ile
ENST00000436117.2:c.803C>T	ENSP00000410980.2:p.Thr268Ile
NM_000245.2:c.803C>T	NP_000236.2:p.Thr268Ile
NM_001127500.1:c.803C>T , LRG_662t1:c.803C>T	NP_001120972.1:p.Thr268Ile
XM_006715991.2:c.-91+27310C>T	XP_006716054.1:n.-91+27310C>T
XM_011516223.1:c.860C>T	XP_011514525.1:p.Thr287Ile
NM_000245.3:c.803C>T	NP_000236.2:p.Thr268Ile
NM_001127500.2:c.803C>T	NP_001120972.1:p.Thr268Ile
NM_001324401.1:c.803C>T	NP_001311330.1:p.Thr268Ile
NM_001324402.1:c.-91+27310C>T	NP_001311331.1:n.-91+27310C>T
XR_001744772.1:n.1034C>T
NM_001127500.3:c.803C>T	NP_001120972.1:p.Thr268Ile
NM_000245.4:c.803C>T MANE Select	NP_000236.2:p.Thr268Ile
NM_001324401.2:c.803C>T	NP_001311330.1:p.Thr268Ile
NM_001324402.2:c.-91+27310C>T	NP_001311331.1:n.-91+27310C>T
NM_001324401.3:c.803C>T	NP_001311330.1:p.Thr268Ile