Canonical Allele Identifier: CA257000

Gene: MET

Linked Data

• ClinVar Variation Id: 13884
• ClinVar RCV Id: RCV000014898 ; RCV000420939
• dbSNP Id: rs121913671
• COSMIC: COSM5015794
• MyVariant Identifiers: chr7:g.116423407G>A (hg19) ; chr7:g.116783353G>A (hg38)
• CIViC: CA257000
• PubMed: PMID:9140397 ; PMID:9826708

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783353G>A , CM000669.2:g.116783353G>A	GRCh38
NC_000007.13:g.116423407G>A , CM000669.1:g.116423407G>A	GRCh37
NC_000007.12:g.116210643G>A	NCBI36
NG_008996.1:g.115949G>A , LRG_662:g.115949G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*1287G>A	ENSP00000410980.2:n.*1287G>A
ENST00000318493.11:c.3736G>A	ENSP00000317272.6:p.Asp1246Asn
ENST00000397752.8:c.3682G>A MANE Select	ENSP00000380860.3:p.Asp1228Asn
ENST00000318493.10:c.3736G>A	ENSP00000317272.6:p.Asp1246Asn
ENST00000397752.7:c.3682G>A	ENSP00000380860.3:p.Asp1228Asn
NM_000245.2:c.3682G>A	NP_000236.2:p.Asp1228Asn
NM_001127500.1:c.3736G>A , LRG_662t1:c.3736G>A	NP_001120972.1:p.Asp1246Asn
XM_006715990.2:c.2392G>A	XP_006716053.1:p.Asp798Asn
XM_006715991.2:c.2392G>A	XP_006716054.1:p.Asp798Asn
XM_011516223.1:c.3739G>A	XP_011514525.1:p.Asp1247Asn
NM_000245.3:c.3682G>A	NP_000236.2:p.Asp1228Asn
NM_001127500.2:c.3736G>A	NP_001120972.1:p.Asp1246Asn
NM_001324402.1:c.2392G>A	NP_001311331.1:p.Asp798Asn
XR_001744772.1:n.3813G>A
NM_001127500.3:c.3736G>A	NP_001120972.1:p.Asp1246Asn
NM_000245.4:c.3682G>A MANE Select	NP_000236.2:p.Asp1228Asn
NM_001324402.2:c.2392G>A	NP_001311331.1:p.Asp798Asn