Canonical Allele Identifier: CA369118216

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116795967C>T , CM000669.2:g.116795967C>T	GRCh38
NC_000007.13:g.116436021C>T , CM000669.1:g.116436021C>T	GRCh37
NC_000007.12:g.116223257C>T	NCBI36
NG_008996.1:g.128563C>T , LRG_662:g.128563C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*1621C>T	ENSP00000410980.2:n.*1621C>T
ENST00000318493.11:c.4070C>T	ENSP00000317272.6:p.Ala1357Val
ENST00000397752.8:c.4016C>T MANE Select	ENSP00000380860.3:p.Ala1339Val
ENST00000318493.10:c.4070C>T	ENSP00000317272.6:p.Ala1357Val
ENST00000397752.7:c.4016C>T	ENSP00000380860.3:p.Ala1339Val
NM_000245.2:c.4016C>T	NP_000236.2:p.Ala1339Val
NM_001127500.1:c.4070C>T , LRG_662t1:c.4070C>T	NP_001120972.1:p.Ala1357Val
XM_006715990.2:c.2726C>T	XP_006716053.1:p.Ala909Val
XM_006715991.2:c.2726C>T	XP_006716054.1:p.Ala909Val
XM_011516223.1:c.4073C>T	XP_011514525.1:p.Ala1358Val
NM_000245.3:c.4016C>T	NP_000236.2:p.Ala1339Val
NM_001127500.2:c.4070C>T	NP_001120972.1:p.Ala1357Val
NM_001324402.1:c.2726C>T	NP_001311331.1:p.Ala909Val
XR_001744772.1:n.4147C>T
NM_001127500.3:c.4070C>T	NP_001120972.1:p.Ala1357Val
NM_000245.4:c.4016C>T MANE Select	NP_000236.2:p.Ala1339Val
NM_001324402.2:c.2726C>T	NP_001311331.1:p.Ala909Val