Canonical Allele Identifier: CA10623054

Gene: MET

Linked Data

• ClinVar Variation Id: 358688
• ClinVar RCV Id: RCV000366689 ; RCV003761942
• dbSNP Id: rs780230492
• MyVariant Identifiers: chr7:g.116397604T>G (hg19) ; chr7:g.116757550T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116757550T>G , CM000669.2:g.116757550T>G	GRCh38
NC_000007.13:g.116397604T>G , CM000669.1:g.116397604T>G	GRCh37
NC_000007.12:g.116184840T>G	NCBI36
NG_008996.1:g.90146T>G , LRG_662:g.90146T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.1965+11T>G	ENSP00000398776.2:n.1965+11T>G
ENST00000436117.3:c.1965+11T>G	ENSP00000410980.2:n.1965+11T>G
ENST00000318493.11:c.1965+11T>G	ENSP00000317272.6:n.1965+11T>G
ENST00000397752.8:c.1965+11T>G MANE Select	ENSP00000380860.3:n.1965+11T>G
ENST00000318493.10:c.1965+11T>G	ENSP00000317272.6:n.1965+11T>G
ENST00000397752.7:c.1965+11T>G	ENSP00000380860.3:n.1965+11T>G
ENST00000436117.2:c.1965+11T>G	ENSP00000410980.2:n.1965+11T>G
NM_000245.2:c.1965+11T>G	NP_000236.2:n.1965+11T>G
NM_001127500.1:c.1965+11T>G , LRG_662t1:c.1965+11T>G	NP_001120972.1:n.1965+11T>G
XM_006715990.2:c.675+11T>G	XP_006716053.1:n.675+11T>G
XM_006715991.2:c.675+11T>G	XP_006716054.1:n.675+11T>G
XM_011516223.1:c.2022+11T>G	XP_011514525.1:n.2022+11T>G
NM_000245.3:c.1965+11T>G	NP_000236.2:n.1965+11T>G
NM_001127500.2:c.1965+11T>G	NP_001120972.1:n.1965+11T>G
NM_001324401.1:c.1965+11T>G	NP_001311330.1:n.1965+11T>G
NM_001324402.1:c.675+11T>G	NP_001311331.1:n.675+11T>G
XR_001744772.1:n.2196+11T>G
NM_001127500.3:c.1965+11T>G	NP_001120972.1:n.1965+11T>G
NM_000245.4:c.1965+11T>G MANE Select	NP_000236.2:n.1965+11T>G
NM_001324401.2:c.1965+11T>G	NP_001311330.1:n.1965+11T>G
NM_001324402.2:c.675+11T>G	NP_001311331.1:n.675+11T>G
NM_001324401.3:c.1965+11T>G	NP_001311330.1:n.1965+11T>G