Canonical Allele Identifier: CA368983580

Gene: MET

Linked Data

• dbSNP Id: rs1562925733
• MyVariant Identifiers: chr7:g.116403278C>A (hg19) ; chr7:g.116763224C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116763224C>A , CM000669.2:g.116763224C>A	GRCh38
NC_000007.13:g.116403278C>A , CM000669.1:g.116403278C>A	GRCh37
NC_000007.12:g.116190514C>A	NCBI36
NG_008996.1:g.95820C>A , LRG_662:g.95820C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000422097.2:c.2539C>A	ENSP00000398776.2:p.Pro847Thr
ENST00000436117.3:c.*144C>A	ENSP00000410980.2:n.*144C>A
ENST00000318493.11:c.2593C>A	ENSP00000317272.6:p.Pro865Thr
ENST00000397752.8:c.2539C>A MANE Select	ENSP00000380860.3:p.Pro847Thr
ENST00000318493.10:c.2593C>A	ENSP00000317272.6:p.Pro865Thr
ENST00000397752.7:c.2539C>A	ENSP00000380860.3:p.Pro847Thr
ENST00000422097.1:c.379C>A	ENSP00000398776.1:p.Pro127Thr
NM_000245.2:c.2539C>A	NP_000236.2:p.Pro847Thr
NM_001127500.1:c.2593C>A , LRG_662t1:c.2593C>A	NP_001120972.1:p.Pro865Thr
XM_006715990.2:c.1249C>A	XP_006716053.1:p.Pro417Thr
XM_006715991.2:c.1249C>A	XP_006716054.1:p.Pro417Thr
XM_011516223.1:c.2596C>A	XP_011514525.1:p.Pro866Thr
NM_000245.3:c.2539C>A	NP_000236.2:p.Pro847Thr
NM_001127500.2:c.2593C>A	NP_001120972.1:p.Pro865Thr
NM_001324401.1:c.2539C>A	NP_001311330.1:p.Pro847Thr
NM_001324402.1:c.1249C>A	NP_001311331.1:p.Pro417Thr
XR_001744772.1:n.2670C>A
NM_001127500.3:c.2593C>A	NP_001120972.1:p.Pro865Thr
NM_000245.4:c.2539C>A MANE Select	NP_000236.2:p.Pro847Thr
NM_001324401.2:c.2539C>A	NP_001311330.1:p.Pro847Thr
NM_001324402.2:c.1249C>A	NP_001311331.1:p.Pro417Thr
NM_001324401.3:c.2539C>A	NP_001311330.1:p.Pro847Thr