Canonical Allele Identifier: CA457219454
Gene: MET HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.116423424A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116783370A>G , CM000669.2:g.116783370A>G GRCh38
NC_000007.13:g.116423424A>G , CM000669.1:g.116423424A>G GRCh37
NC_000007.12:g.116210660A>G NCBI36
NG_008996.1:g.115966A>G , LRG_662:g.115966A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000436117.3:c.*1304A>G ENSP00000410980.2:n.*1304A>G
ENST00000318493.11:c.3753A>G ENSP00000317272.6:p.Glu1251=
ENST00000397752.8:c.3699A>G MANE Select ENSP00000380860.3:p.Glu1233=
ENST00000318493.10:c.3753A>G ENSP00000317272.6:p.Glu1251=
ENST00000397752.7:c.3699A>G ENSP00000380860.3:p.Glu1233=
NM_000245.2:c.3699A>G NP_000236.2:p.Glu1233=
NM_001127500.1:c.3753A>G , LRG_662t1:c.3753A>G NP_001120972.1:p.Glu1251=
XM_006715990.2:c.2409A>G XP_006716053.1:p.Glu803=
XM_006715991.2:c.2409A>G XP_006716054.1:p.Glu803=
XM_011516223.1:c.3756A>G XP_011514525.1:p.Glu1252=
NM_000245.3:c.3699A>G NP_000236.2:p.Glu1233=
NM_001127500.2:c.3753A>G NP_001120972.1:p.Glu1251=
NM_001324402.1:c.2409A>G NP_001311331.1:p.Glu803=
XR_001744772.1:n.3830A>G
NM_001127500.3:c.3753A>G NP_001120972.1:p.Glu1251=
NM_000245.4:c.3699A>G MANE Select NP_000236.2:p.Glu1233=
NM_001324402.2:c.2409A>G NP_001311331.1:p.Glu803=