Canonical Allele Identifier: CA368989614

Gene: MET

Linked Data

• ClinVar Variation Id: 1697562
• ClinVar RCV Id: RCV002268846
• dbSNP Id: rs2117039915
• MyVariant Identifiers: chr7:g.116417469A>G (hg19) ; chr7:g.116777415A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116777415A>G , CM000669.2:g.116777415A>G	GRCh38
NC_000007.13:g.116417469A>G , CM000669.1:g.116417469A>G	GRCh37
NC_000007.12:g.116204705A>G	NCBI36
NG_008996.1:g.110011A>G , LRG_662:g.110011A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*891A>G	ENSP00000410980.2:n.*891A>G
ENST00000318493.11:c.3340A>G	ENSP00000317272.6:p.Thr1114Ala
ENST00000397752.8:c.3286A>G MANE Select	ENSP00000380860.3:p.Thr1096Ala
ENST00000318493.10:c.3340A>G	ENSP00000317272.6:p.Thr1114Ala
ENST00000397752.7:c.3286A>G	ENSP00000380860.3:p.Thr1096Ala
NM_000245.2:c.3286A>G	NP_000236.2:p.Thr1096Ala
NM_001127500.1:c.3340A>G , LRG_662t1:c.3340A>G	NP_001120972.1:p.Thr1114Ala
XM_006715990.2:c.1996A>G	XP_006716053.1:p.Thr666Ala
XM_006715991.2:c.1996A>G	XP_006716054.1:p.Thr666Ala
XM_011516223.1:c.3343A>G	XP_011514525.1:p.Thr1115Ala
NM_000245.3:c.3286A>G	NP_000236.2:p.Thr1096Ala
NM_001127500.2:c.3340A>G	NP_001120972.1:p.Thr1114Ala
NM_001324402.1:c.1996A>G	NP_001311331.1:p.Thr666Ala
XR_001744772.1:n.3417A>G
NM_001127500.3:c.3340A>G	NP_001120972.1:p.Thr1114Ala
NM_000245.4:c.3286A>G MANE Select	NP_000236.2:p.Thr1096Ala
NM_001324402.2:c.1996A>G	NP_001311331.1:p.Thr666Ala