Canonical Allele Identifier: CA10584665

Gene: MET

Linked Data

• ClinVar Variation Id: 246635
• ClinVar RCV Id: RCV001306836
• dbSNP Id: rs879254335
• MyVariant Identifiers: chr7:g.116411685T>A (hg19) ; chr7:g.116771631T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771631T>A , CM000669.2:g.116771631T>A	GRCh38
NC_000007.13:g.116411685T>A , CM000669.1:g.116411685T>A	GRCh37
NC_000007.12:g.116198921T>A	NCBI36
NG_008996.1:g.104227T>A , LRG_662:g.104227T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*469T>A	ENSP00000410980.2:n.*469T>A
ENST00000318493.11:c.2918T>A	ENSP00000317272.6:p.Leu973Gln
ENST00000397752.8:c.2864T>A MANE Select	ENSP00000380860.3:p.Leu955Gln
ENST00000318493.10:c.2918T>A	ENSP00000317272.6:p.Leu973Gln
ENST00000397752.7:c.2864T>A	ENSP00000380860.3:p.Leu955Gln
ENST00000454623.1:c.260T>A	ENSP00000398140.1:p.Leu87Gln
NM_000245.2:c.2864T>A	NP_000236.2:p.Leu955Gln
NM_001127500.1:c.2918T>A , LRG_662t1:c.2918T>A	NP_001120972.1:p.Leu973Gln
XM_006715990.2:c.1574T>A	XP_006716053.1:p.Leu525Gln
XM_006715991.2:c.1574T>A	XP_006716054.1:p.Leu525Gln
XM_011516223.1:c.2921T>A	XP_011514525.1:p.Leu974Gln
NM_000245.3:c.2864T>A	NP_000236.2:p.Leu955Gln
NM_001127500.2:c.2918T>A	NP_001120972.1:p.Leu973Gln
NM_001324402.1:c.1574T>A	NP_001311331.1:p.Leu525Gln
XR_001744772.1:n.2995T>A
NM_001127500.3:c.2918T>A	NP_001120972.1:p.Leu973Gln
NM_000245.4:c.2864T>A MANE Select	NP_000236.2:p.Leu955Gln
NM_001324402.2:c.1574T>A	NP_001311331.1:p.Leu525Gln