Canonical Allele Identifier: CA368991889

Gene: MET

Linked Data

• dbSNP Id: rs121913245
• MyVariant Identifiers: chr7:g.116423474T>A (hg19) ; chr7:g.116783420T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783420T>A , CM000669.2:g.116783420T>A	GRCh38
NC_000007.13:g.116423474T>A , CM000669.1:g.116423474T>A	GRCh37
NC_000007.12:g.116210710T>A	NCBI36
NG_008996.1:g.116016T>A , LRG_662:g.116016T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000436117.3:c.*1354T>A	ENSP00000410980.2:n.*1354T>A
ENST00000318493.11:c.3803T>A	ENSP00000317272.6:p.Met1268Lys
ENST00000397752.8:c.3749T>A MANE Select	ENSP00000380860.3:p.Met1250Lys
ENST00000318493.10:c.3803T>A	ENSP00000317272.6:p.Met1268Lys
ENST00000397752.7:c.3749T>A	ENSP00000380860.3:p.Met1250Lys
NM_000245.2:c.3749T>A	NP_000236.2:p.Met1250Lys
NM_001127500.1:c.3803T>A , LRG_662t1:c.3803T>A	NP_001120972.1:p.Met1268Lys
XM_006715990.2:c.2459T>A	XP_006716053.1:p.Met820Lys
XM_006715991.2:c.2459T>A	XP_006716054.1:p.Met820Lys
XM_011516223.1:c.3806T>A	XP_011514525.1:p.Met1269Lys
NM_000245.3:c.3749T>A	NP_000236.2:p.Met1250Lys
NM_001127500.2:c.3803T>A	NP_001120972.1:p.Met1268Lys
NM_001324402.1:c.2459T>A	NP_001311331.1:p.Met820Lys
XR_001744772.1:n.3880T>A
NM_001127500.3:c.3803T>A	NP_001120972.1:p.Met1268Lys
NM_000245.4:c.3749T>A MANE Select	NP_000236.2:p.Met1250Lys
NM_001324402.2:c.2459T>A	NP_001311331.1:p.Met820Lys