Canonical Allele Identifier: CA2580076357

Gene: MET

Linked Data

• ClinVar Variation Id: 2120468
• ClinVar RCV Id: RCV003059396
• dbSNP Id: rs2116995521

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771831C>G , CM000669.2:g.116771831C>G	GRCh38
NC_000007.13:g.116411885C>G , CM000669.1:g.116411885C>G	GRCh37
NC_000007.12:g.116199121C>G	NCBI36
NG_008996.1:g.104427C>G , LRG_662:g.104427C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*493-18C>G	ENSP00000410980.2:n.*493-18C>G
ENST00000318493.11:c.2942-18C>G	ENSP00000317272.6:n.2942-18C>G
ENST00000397752.8:c.2888-18C>G MANE Select	ENSP00000380860.3:n.2888-18C>G
ENST00000318493.10:c.2942-18C>G	ENSP00000317272.6:n.2942-18C>G
ENST00000397752.7:c.2888-18C>G	ENSP00000380860.3:n.2888-18C>G
ENST00000454623.1:c.283+177C>G	ENSP00000398140.1:n.283+177C>G
NM_000245.2:c.2888-18C>G	NP_000236.2:n.2888-18C>G
NM_001127500.1:c.2942-18C>G , LRG_662t1:c.2942-18C>G	NP_001120972.1:n.2942-18C>G
XM_006715990.2:c.1598-18C>G	XP_006716053.1:n.1598-18C>G
XM_006715991.2:c.1598-18C>G	XP_006716054.1:n.1598-18C>G
XM_011516223.1:c.2945-18C>G	XP_011514525.1:n.2945-18C>G
NM_000245.3:c.2888-18C>G	NP_000236.2:n.2888-18C>G
NM_001127500.2:c.2942-18C>G	NP_001120972.1:n.2942-18C>G
NM_001324402.1:c.1598-18C>G	NP_001311331.1:n.1598-18C>G
XR_001744772.1:n.3019-18C>G
NM_001127500.3:c.2942-18C>G	NP_001120972.1:n.2942-18C>G
NM_000245.4:c.2888-18C>G MANE Select	NP_000236.2:n.2888-18C>G
NM_001324402.2:c.1598-18C>G	NP_001311331.1:n.1598-18C>G