Canonical Allele Identifier: CA368989664

Gene: MET

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116777427A>G , CM000669.2:g.116777427A>G	GRCh38
NC_000007.13:g.116417481A>G , CM000669.1:g.116417481A>G	GRCh37
NC_000007.12:g.116204717A>G	NCBI36
NG_008996.1:g.110023A>G , LRG_662:g.110023A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*903A>G	ENSP00000410980.2:n.*903A>G
ENST00000318493.11:c.3352A>G	ENSP00000317272.6:p.Asn1118Asp
ENST00000397752.8:c.3298A>G MANE Select	ENSP00000380860.3:p.Asn1100Asp
ENST00000318493.10:c.3352A>G	ENSP00000317272.6:p.Asn1118Asp
ENST00000397752.7:c.3298A>G	ENSP00000380860.3:p.Asn1100Asp
NM_000245.2:c.3298A>G	NP_000236.2:p.Asn1100Asp
NM_001127500.1:c.3352A>G , LRG_662t1:c.3352A>G	NP_001120972.1:p.Asn1118Asp
XM_006715990.2:c.2008A>G	XP_006716053.1:p.Asn670Asp
XM_006715991.2:c.2008A>G	XP_006716054.1:p.Asn670Asp
XM_011516223.1:c.3355A>G	XP_011514525.1:p.Asn1119Asp
NM_000245.3:c.3298A>G	NP_000236.2:p.Asn1100Asp
NM_001127500.2:c.3352A>G	NP_001120972.1:p.Asn1118Asp
NM_001324402.1:c.2008A>G	NP_001311331.1:p.Asn670Asp
XR_001744772.1:n.3429A>G
NM_001127500.3:c.3352A>G	NP_001120972.1:p.Asn1118Asp
NM_000245.4:c.3298A>G MANE Select	NP_000236.2:p.Asn1100Asp
NM_001324402.2:c.2008A>G	NP_001311331.1:p.Asn670Asp