Canonical Allele Identifier: CA368991080

Gene: MET

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116782048C>A , CM000669.2:g.116782048C>A	GRCh38
NC_000007.13:g.116422102C>A , CM000669.1:g.116422102C>A	GRCh37
NC_000007.12:g.116209338C>A	NCBI36
NG_008996.1:g.114644C>A , LRG_662:g.114644C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*1188C>A	ENSP00000410980.2:n.*1188C>A
ENST00000318493.11:c.3637C>A	ENSP00000317272.6:p.Leu1213Ile
ENST00000397752.8:c.3583C>A MANE Select	ENSP00000380860.3:p.Leu1195Ile
ENST00000318493.10:c.3637C>A	ENSP00000317272.6:p.Leu1213Ile
ENST00000397752.7:c.3583C>A	ENSP00000380860.3:p.Leu1195Ile
NM_000245.2:c.3583C>A	NP_000236.2:p.Leu1195Ile
NM_001127500.1:c.3637C>A , LRG_662t1:c.3637C>A	NP_001120972.1:p.Leu1213Ile
XM_006715990.2:c.2293C>A	XP_006716053.1:p.Leu765Ile
XM_006715991.2:c.2293C>A	XP_006716054.1:p.Leu765Ile
XM_011516223.1:c.3640C>A	XP_011514525.1:p.Leu1214Ile
NM_000245.3:c.3583C>A	NP_000236.2:p.Leu1195Ile
NM_001127500.2:c.3637C>A	NP_001120972.1:p.Leu1213Ile
NM_001324402.1:c.2293C>A	NP_001311331.1:p.Leu765Ile
XR_001744772.1:n.3714C>A
NM_001127500.3:c.3637C>A	NP_001120972.1:p.Leu1213Ile
NM_000245.4:c.3583C>A MANE Select	NP_000236.2:p.Leu1195Ile
NM_001324402.2:c.2293C>A	NP_001311331.1:p.Leu765Ile