Canonical Allele Identifier: CA368982540

Gene: MET

Linked Data

• ClinVar Variation Id: 2567696
• ClinVar RCV Id: RCV003278635
• gnomAD v4: 7-116759479-A-G
• MyVariant Identifiers: chr7:g.116399533A>G (hg19) ; chr7:g.116759479A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759479A>G , CM000669.2:g.116759479A>G	GRCh38
NC_000007.13:g.116399533A>G , CM000669.1:g.116399533A>G	GRCh37
NC_000007.12:g.116186769A>G	NCBI36
NG_008996.1:g.92075A>G , LRG_662:g.92075A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2353A>G	ENSP00000398776.2:p.Asn785Asp
ENST00000436117.3:c.2264+859A>G	ENSP00000410980.2:n.2264+859A>G
ENST00000318493.11:c.2407A>G	ENSP00000317272.6:p.Asn803Asp
ENST00000397752.8:c.2353A>G MANE Select	ENSP00000380860.3:p.Asn785Asp
ENST00000318493.10:c.2407A>G	ENSP00000317272.6:p.Asn803Asp
ENST00000397752.7:c.2353A>G	ENSP00000380860.3:p.Asn785Asp
ENST00000422097.1:c.193A>G	ENSP00000398776.1:p.Asn65Asp
ENST00000436117.2:c.2264+859A>G	ENSP00000410980.2:n.2264+859A>G
NM_000245.2:c.2353A>G	NP_000236.2:p.Asn785Asp
NM_001127500.1:c.2407A>G , LRG_662t1:c.2407A>G	NP_001120972.1:p.Asn803Asp
XM_006715990.2:c.1063A>G	XP_006716053.1:p.Asn355Asp
XM_006715991.2:c.1063A>G	XP_006716054.1:p.Asn355Asp
XM_011516223.1:c.2410A>G	XP_011514525.1:p.Asn804Asp
NM_000245.3:c.2353A>G	NP_000236.2:p.Asn785Asp
NM_001127500.2:c.2407A>G	NP_001120972.1:p.Asn803Asp
NM_001324401.1:c.2353A>G	NP_001311330.1:p.Asn785Asp
NM_001324402.1:c.1063A>G	NP_001311331.1:p.Asn355Asp
XR_001744772.1:n.2495+859A>G
NM_001127500.3:c.2407A>G	NP_001120972.1:p.Asn803Asp
NM_000245.4:c.2353A>G MANE Select	NP_000236.2:p.Asn785Asp
NM_001324401.2:c.2353A>G	NP_001311330.1:p.Asn785Asp
NM_001324402.2:c.1063A>G	NP_001311331.1:p.Asn355Asp
NM_001324401.3:c.2353A>G	NP_001311330.1:p.Asn785Asp