Canonical Allele Identifier: CA368982386

Gene: MET

Linked Data

• ClinVar Variation Id: 1790456
• ClinVar RCV Id: RCV002457909
• MyVariant Identifiers: chr7:g.116399507T>G (hg19) ; chr7:g.116759453T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759453T>G , CM000669.2:g.116759453T>G	GRCh38
NC_000007.13:g.116399507T>G , CM000669.1:g.116399507T>G	GRCh37
NC_000007.12:g.116186743T>G	NCBI36
NG_008996.1:g.92049T>G , LRG_662:g.92049T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2327T>G	ENSP00000398776.2:p.Val776Gly
ENST00000436117.3:c.2264+833T>G	ENSP00000410980.2:n.2264+833T>G
ENST00000318493.11:c.2381T>G	ENSP00000317272.6:p.Val794Gly
ENST00000397752.8:c.2327T>G MANE Select	ENSP00000380860.3:p.Val776Gly
ENST00000318493.10:c.2381T>G	ENSP00000317272.6:p.Val794Gly
ENST00000397752.7:c.2327T>G	ENSP00000380860.3:p.Val776Gly
ENST00000422097.1:c.167T>G	ENSP00000398776.1:p.Val56Gly
ENST00000436117.2:c.2264+833T>G	ENSP00000410980.2:n.2264+833T>G
NM_000245.2:c.2327T>G	NP_000236.2:p.Val776Gly
NM_001127500.1:c.2381T>G , LRG_662t1:c.2381T>G	NP_001120972.1:p.Val794Gly
XM_006715990.2:c.1037T>G	XP_006716053.1:p.Val346Gly
XM_006715991.2:c.1037T>G	XP_006716054.1:p.Val346Gly
XM_011516223.1:c.2384T>G	XP_011514525.1:p.Val795Gly
NM_000245.3:c.2327T>G	NP_000236.2:p.Val776Gly
NM_001127500.2:c.2381T>G	NP_001120972.1:p.Val794Gly
NM_001324401.1:c.2327T>G	NP_001311330.1:p.Val776Gly
NM_001324402.1:c.1037T>G	NP_001311331.1:p.Val346Gly
XR_001744772.1:n.2495+833T>G
NM_001127500.3:c.2381T>G	NP_001120972.1:p.Val794Gly
NM_000245.4:c.2327T>G MANE Select	NP_000236.2:p.Val776Gly
NM_001324401.2:c.2327T>G	NP_001311330.1:p.Val776Gly
NM_001324402.2:c.1037T>G	NP_001311331.1:p.Val346Gly
NM_001324401.3:c.2327T>G	NP_001311330.1:p.Val776Gly