Canonical Allele Identifier: CA368983529
Gene: MET HGNC NCBI

Linked Data

dbSNP Id: rs2116956566

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116763210A>G , CM000669.2:g.116763210A>G GRCh38
NC_000007.13:g.116403264A>G , CM000669.1:g.116403264A>G GRCh37
NC_000007.12:g.116190500A>G NCBI36
NG_008996.1:g.95806A>G , LRG_662:g.95806A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000422097.2:c.2525A>G ENSP00000398776.2:p.Lys842Arg
ENST00000436117.3:c.*130A>G ENSP00000410980.2:n.*130A>G
ENST00000318493.11:c.2579A>G ENSP00000317272.6:p.Lys860Arg
ENST00000397752.8:c.2525A>G MANE Select ENSP00000380860.3:p.Lys842Arg
ENST00000318493.10:c.2579A>G ENSP00000317272.6:p.Lys860Arg
ENST00000397752.7:c.2525A>G ENSP00000380860.3:p.Lys842Arg
ENST00000422097.1:c.365A>G ENSP00000398776.1:p.Lys122Arg
NM_000245.2:c.2525A>G NP_000236.2:p.Lys842Arg
NM_001127500.1:c.2579A>G , LRG_662t1:c.2579A>G NP_001120972.1:p.Lys860Arg
XM_006715990.2:c.1235A>G XP_006716053.1:p.Lys412Arg
XM_006715991.2:c.1235A>G XP_006716054.1:p.Lys412Arg
XM_011516223.1:c.2582A>G XP_011514525.1:p.Lys861Arg
NM_000245.3:c.2525A>G NP_000236.2:p.Lys842Arg
NM_001127500.2:c.2579A>G NP_001120972.1:p.Lys860Arg
NM_001324401.1:c.2525A>G NP_001311330.1:p.Lys842Arg
NM_001324402.1:c.1235A>G NP_001311331.1:p.Lys412Arg
XR_001744772.1:n.2656A>G
NM_001127500.3:c.2579A>G NP_001120972.1:p.Lys860Arg
NM_000245.4:c.2525A>G MANE Select NP_000236.2:p.Lys842Arg
NM_001324401.2:c.2525A>G NP_001311330.1:p.Lys842Arg
NM_001324402.2:c.1235A>G NP_001311331.1:p.Lys412Arg
NM_001324401.3:c.2525A>G NP_001311330.1:p.Lys842Arg