Canonical Allele Identifier: CA392937302
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140675022
COSMIC: COSM5849602
MyVariant Identifiers: chr15:g.66777460G>T (hg19) chr15:g.66485122G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485122G>T , CM000677.2:g.66485122G>T GRCh38
NC_000015.9:g.66777460G>T , CM000677.1:g.66777460G>T GRCh37
NC_000015.8:g.64564514G>T NCBI36
NG_008305.1:g.103250G>T , LRG_725:g.103250G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2106G>T ENSP00000508681.1:n.628-2106G>T
ENST00000685172.1:c.826G>T ENSP00000509604.1:p.Gly276Trp
ENST00000685763.1:c.679G>T ENSP00000509016.1:p.Gly227Trp
ENST00000686347.1:c.569-2106G>T ENSP00000509027.1:n.569-2106G>T
ENST00000687191.1:n.1184G>T
ENST00000687481.1:n.241G>T
ENST00000689951.1:c.877G>T ENSP00000509308.1:p.Gly293Trp
ENST00000691077.1:c.*63G>T ENSP00000509843.1:n.*63G>T
ENST00000691576.1:c.697G>T ENSP00000510066.1:p.Gly233Trp
ENST00000691937.1:c.826G>T ENSP00000508768.1:p.Gly276Trp
ENST00000692487.1:c.*63G>T ENSP00000509534.1:n.*63G>T
ENST00000692683.1:c.760G>T ENSP00000508437.1:p.Gly254Trp
ENST00000693150.1:c.682G>T ENSP00000510309.1:p.Gly228Trp
ENST00000307102.10:c.826G>T MANE Select ENSP00000302486.5:p.Gly276Trp
ENST00000307102.9:c.826G>T ENSP00000302486.4:p.Gly276Trp
ENST00000566326.1:c.298G>T ENSP00000456438.1:p.Gly100Trp
NM_002755.3:c.826G>T , LRG_725t1:c.826G>T NP_002746.1:p.Gly276Trp
XM_011521783.1:c.760G>T XP_011520085.1:p.Gly254Trp
XM_011521783.3:c.760G>T XP_011520085.1:p.Gly254Trp
XM_017022411.2:c.748G>T XP_016877900.1:p.Gly250Trp
XM_017022412.1:c.682G>T XP_016877901.1:p.Gly228Trp
XM_017022413.1:c.298G>T XP_016877902.1:p.Gly100Trp
NM_002755.4:c.826G>T MANE Select NP_002746.1:p.Gly276Trp
Search 100 bp 5'
Search 100 bp 3'