Canonical Allele Identifier: CA392937327
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140675118
MyVariant Identifiers: chr15:g.66777472G>A (hg19) chr15:g.66485134G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485134G>A , CM000677.2:g.66485134G>A GRCh38
NC_000015.9:g.66777472G>A , CM000677.1:g.66777472G>A GRCh37
NC_000015.8:g.64564526G>A NCBI36
NG_008305.1:g.103262G>A , LRG_725:g.103262G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2094G>A ENSP00000508681.1:n.628-2094G>A
ENST00000685172.1:c.838G>A ENSP00000509604.1:p.Glu280Lys
ENST00000685763.1:c.691G>A ENSP00000509016.1:p.Glu231Lys
ENST00000686347.1:c.569-2094G>A ENSP00000509027.1:n.569-2094G>A
ENST00000687191.1:n.1196G>A
ENST00000687481.1:n.253G>A
ENST00000689951.1:c.889G>A ENSP00000509308.1:p.Glu297Lys
ENST00000691077.1:c.*75G>A ENSP00000509843.1:n.*75G>A
ENST00000691576.1:c.709G>A ENSP00000510066.1:p.Glu237Lys
ENST00000691937.1:c.838G>A ENSP00000508768.1:p.Glu280Lys
ENST00000692487.1:c.*75G>A ENSP00000509534.1:n.*75G>A
ENST00000692683.1:c.772G>A ENSP00000508437.1:p.Glu258Lys
ENST00000693150.1:c.694G>A ENSP00000510309.1:p.Glu232Lys
ENST00000307102.10:c.838G>A MANE Select ENSP00000302486.5:p.Glu280Lys
ENST00000307102.9:c.838G>A ENSP00000302486.4:p.Glu280Lys
ENST00000566326.1:c.310G>A ENSP00000456438.1:p.Glu104Lys
NM_002755.3:c.838G>A , LRG_725t1:c.838G>A NP_002746.1:p.Glu280Lys
XM_011521783.1:c.772G>A XP_011520085.1:p.Glu258Lys
XM_011521783.3:c.772G>A XP_011520085.1:p.Glu258Lys
XM_017022411.2:c.760G>A XP_016877900.1:p.Glu254Lys
XM_017022412.1:c.694G>A XP_016877901.1:p.Glu232Lys
XM_017022413.1:c.310G>A XP_016877902.1:p.Glu104Lys
NM_002755.4:c.838G>A MANE Select NP_002746.1:p.Glu280Lys
Search 100 bp 5'
Search 100 bp 3'