Canonical Allele Identifier: CA368991575

Gene: MET

Linked Data

• ClinVar Variation Id: 1734439
• ClinVar RCV Id: RCV002349214
• dbSNP Id: rs786201612
• MyVariant Identifiers: chr7:g.116423409C>G (hg19) ; chr7:g.116783355C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783355C>G , CM000669.2:g.116783355C>G	GRCh38
NC_000007.13:g.116423409C>G , CM000669.1:g.116423409C>G	GRCh37
NC_000007.12:g.116210645C>G	NCBI36
NG_008996.1:g.115951C>G , LRG_662:g.115951C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000436117.3:c.*1289C>G	ENSP00000410980.2:n.*1289C>G
ENST00000318493.11:c.3738C>G	ENSP00000317272.6:p.Asp1246Glu
ENST00000397752.8:c.3684C>G MANE Select	ENSP00000380860.3:p.Asp1228Glu
ENST00000318493.10:c.3738C>G	ENSP00000317272.6:p.Asp1246Glu
ENST00000397752.7:c.3684C>G	ENSP00000380860.3:p.Asp1228Glu
NM_000245.2:c.3684C>G	NP_000236.2:p.Asp1228Glu
NM_001127500.1:c.3738C>G , LRG_662t1:c.3738C>G	NP_001120972.1:p.Asp1246Glu
XM_006715990.2:c.2394C>G	XP_006716053.1:p.Asp798Glu
XM_006715991.2:c.2394C>G	XP_006716054.1:p.Asp798Glu
XM_011516223.1:c.3741C>G	XP_011514525.1:p.Asp1247Glu
NM_000245.3:c.3684C>G	NP_000236.2:p.Asp1228Glu
NM_001127500.2:c.3738C>G	NP_001120972.1:p.Asp1246Glu
NM_001324402.1:c.2394C>G	NP_001311331.1:p.Asp798Glu
XR_001744772.1:n.3815C>G
NM_001127500.3:c.3738C>G	NP_001120972.1:p.Asp1246Glu
NM_000245.4:c.3684C>G MANE Select	NP_000236.2:p.Asp1228Glu
NM_001324402.2:c.2394C>G	NP_001311331.1:p.Asp798Glu