Canonical Allele Identifier: CA368989621

Gene: MET

Linked Data

• ClinVar Variation Id: 651432
• ClinVar RCV Id: RCV002235306
• dbSNP Id: rs45592846
• MyVariant Identifiers: chr7:g.116417470C>T (hg19) ; chr7:g.116777416C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116777416C>T , CM000669.2:g.116777416C>T	GRCh38
NC_000007.13:g.116417470C>T , CM000669.1:g.116417470C>T	GRCh37
NC_000007.12:g.116204706C>T	NCBI36
NG_008996.1:g.110012C>T , LRG_662:g.110012C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*892C>T	ENSP00000410980.2:n.*892C>T
ENST00000318493.11:c.3341C>T	ENSP00000317272.6:p.Thr1114Ile
ENST00000397752.8:c.3287C>T MANE Select	ENSP00000380860.3:p.Thr1096Ile
ENST00000318493.10:c.3341C>T	ENSP00000317272.6:p.Thr1114Ile
ENST00000397752.7:c.3287C>T	ENSP00000380860.3:p.Thr1096Ile
NM_000245.2:c.3287C>T	NP_000236.2:p.Thr1096Ile
NM_001127500.1:c.3341C>T , LRG_662t1:c.3341C>T	NP_001120972.1:p.Thr1114Ile
XM_006715990.2:c.1997C>T	XP_006716053.1:p.Thr666Ile
XM_006715991.2:c.1997C>T	XP_006716054.1:p.Thr666Ile
XM_011516223.1:c.3344C>T	XP_011514525.1:p.Thr1115Ile
NM_000245.3:c.3287C>T	NP_000236.2:p.Thr1096Ile
NM_001127500.2:c.3341C>T	NP_001120972.1:p.Thr1114Ile
NM_001324402.1:c.1997C>T	NP_001311331.1:p.Thr666Ile
XR_001744772.1:n.3418C>T
NM_001127500.3:c.3341C>T	NP_001120972.1:p.Thr1114Ile
NM_000245.4:c.3287C>T MANE Select	NP_000236.2:p.Thr1096Ile
NM_001324402.2:c.1997C>T	NP_001311331.1:p.Thr666Ile