Canonical Allele Identifier: CA368983182

Gene: MET

Linked Data

• MyVariant Identifiers: chr7:g.116403175A>T (hg19) ; chr7:g.116763121A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116763121A>T , CM000669.2:g.116763121A>T	GRCh38
NC_000007.13:g.116403175A>T , CM000669.1:g.116403175A>T	GRCh37
NC_000007.12:g.116190411A>T	NCBI36
NG_008996.1:g.95717A>T , LRG_662:g.95717A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000422097.2:c.2436A>T	ENSP00000398776.2:p.Gln812His
ENST00000436117.3:c.*41A>T	ENSP00000410980.2:n.*41A>T
ENST00000318493.11:c.2490A>T	ENSP00000317272.6:p.Gln830His
ENST00000397752.8:c.2436A>T MANE Select	ENSP00000380860.3:p.Gln812His
ENST00000318493.10:c.2490A>T	ENSP00000317272.6:p.Gln830His
ENST00000397752.7:c.2436A>T	ENSP00000380860.3:p.Gln812His
ENST00000422097.1:c.276A>T	ENSP00000398776.1:p.Gln92His
NM_000245.2:c.2436A>T	NP_000236.2:p.Gln812His
NM_001127500.1:c.2490A>T , LRG_662t1:c.2490A>T	NP_001120972.1:p.Gln830His
XM_006715990.2:c.1146A>T	XP_006716053.1:p.Gln382His
XM_006715991.2:c.1146A>T	XP_006716054.1:p.Gln382His
XM_011516223.1:c.2493A>T	XP_011514525.1:p.Gln831His
NM_000245.3:c.2436A>T	NP_000236.2:p.Gln812His
NM_001127500.2:c.2490A>T	NP_001120972.1:p.Gln830His
NM_001324401.1:c.2436A>T	NP_001311330.1:p.Gln812His
NM_001324402.1:c.1146A>T	NP_001311331.1:p.Gln382His
XR_001744772.1:n.2567A>T
NM_001127500.3:c.2490A>T	NP_001120972.1:p.Gln830His
NM_000245.4:c.2436A>T MANE Select	NP_000236.2:p.Gln812His
NM_001324401.2:c.2436A>T	NP_001311330.1:p.Gln812His
NM_001324402.2:c.1146A>T	NP_001311331.1:p.Gln382His
NM_001324401.3:c.2436A>T	NP_001311330.1:p.Gln812His