Canonical Allele Identifier: CA4448789

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116795698C>G , CM000669.2:g.116795698C>G	GRCh38
NC_000007.13:g.116435752C>G , CM000669.1:g.116435752C>G	GRCh37
NC_000007.12:g.116222988C>G	NCBI36
NG_008996.1:g.128294C>G , LRG_662:g.128294C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000245.4:c.3842C>G MANE Select	NP_000236.2:p.Ala1281Gly
ENST00000397752.8:c.3842C>G MANE Select	ENSP00000380860.3:p.Ala1281Gly
NM_000245.2:c.3842C>G	NP_000236.2:p.Ala1281Gly
NM_000245.3:c.3842C>G	NP_000236.2:p.Ala1281Gly
NM_001127500.1:c.3896C>G , LRG_662t1:c.3896C>G	NP_001120972.1:p.Ala1299Gly
NM_001127500.2:c.3896C>G	NP_001120972.1:p.Ala1299Gly
NM_001127500.3:c.3896C>G	NP_001120972.1:p.Ala1299Gly
NM_001324402.1:c.2552C>G	NP_001311331.1:p.Ala851Gly
NM_001324402.2:c.2552C>G	NP_001311331.1:p.Ala851Gly
ENST00000318493.10:c.3896C>G	ENSP00000317272.6:p.Ala1299Gly
ENST00000318493.11:c.3896C>G	ENSP00000317272.6:p.Ala1299Gly
ENST00000397752.7:c.3842C>G	ENSP00000380860.3:p.Ala1281Gly
ENST00000436117.3:c.*1447C>G	ENSP00000410980.2:n.*1447C>G
XM_006715990.2:c.2552C>G	XP_006716053.1:p.Ala851Gly
XM_006715991.2:c.2552C>G	XP_006716054.1:p.Ala851Gly
XM_011516223.1:c.3899C>G	XP_011514525.1:p.Ala1300Gly
XR_001744772.1:n.3973C>G