Canonical Allele Identifier: CA350109

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116796051C>G , CM000669.2:g.116796051C>G	GRCh38
NC_000007.13:g.116436105C>G , CM000669.1:g.116436105C>G	GRCh37
NC_000007.12:g.116223341C>G	NCBI36
NG_008996.1:g.128647C>G , LRG_662:g.128647C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*1705C>G	ENSP00000410980.2:n.*1705C>G
ENST00000318493.11:c.4154C>G	ENSP00000317272.6:p.Ser1385Cys
ENST00000397752.8:c.4100C>G MANE Select	ENSP00000380860.3:p.Ser1367Cys
ENST00000318493.10:c.4154C>G	ENSP00000317272.6:p.Ser1385Cys
ENST00000397752.7:c.4100C>G	ENSP00000380860.3:p.Ser1367Cys
NM_000245.2:c.4100C>G	NP_000236.2:p.Ser1367Cys
NM_001127500.1:c.4154C>G , LRG_662t1:c.4154C>G	NP_001120972.1:p.Ser1385Cys
XM_006715990.2:c.2810C>G	XP_006716053.1:p.Ser937Cys
XM_006715991.2:c.2810C>G	XP_006716054.1:p.Ser937Cys
XM_011516223.1:c.4157C>G	XP_011514525.1:p.Ser1386Cys
NM_000245.3:c.4100C>G	NP_000236.2:p.Ser1367Cys
NM_001127500.2:c.4154C>G	NP_001120972.1:p.Ser1385Cys
NM_001324402.1:c.2810C>G	NP_001311331.1:p.Ser937Cys
XR_001744772.1:n.4231C>G
NM_001127500.3:c.4154C>G	NP_001120972.1:p.Ser1385Cys
NM_000245.4:c.4100C>G MANE Select	NP_000236.2:p.Ser1367Cys
NM_001324402.2:c.2810C>G	NP_001311331.1:p.Ser937Cys