Canonical Allele Identifier: CA392936473
Gene: MAP2K1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.66774193C>A (hg19) chr15:g.66481855C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481855C>A , CM000677.2:g.66481855C>A GRCh38
NC_000015.9:g.66774193C>A , CM000677.1:g.66774193C>A GRCh37
NC_000015.8:g.64561247C>A NCBI36
NG_008305.1:g.99983C>A , LRG_725:g.99983C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.603C>A ENSP00000508681.1:p.Phe201Leu
ENST00000685172.1:c.669C>A ENSP00000509604.1:p.Phe223Leu
ENST00000685763.1:c.522C>A ENSP00000509016.1:p.Phe174Leu
ENST00000686347.1:c.569-5373C>A ENSP00000509027.1:n.569-5373C>A
ENST00000687191.1:n.1027C>A
ENST00000689951.1:c.720C>A ENSP00000509308.1:p.Phe240Leu
ENST00000691077.1:c.669C>A ENSP00000509843.1:p.Phe223Leu
ENST00000691576.1:c.569-3139C>A ENSP00000510066.1:n.569-3139C>A
ENST00000691937.1:c.669C>A ENSP00000508768.1:p.Phe223Leu
ENST00000692487.1:c.669C>A ENSP00000509534.1:p.Phe223Leu
ENST00000692683.1:c.603C>A ENSP00000508437.1:p.Phe201Leu
ENST00000693150.1:c.525C>A ENSP00000510309.1:p.Phe175Leu
ENST00000307102.10:c.669C>A MANE Select ENSP00000302486.5:p.Phe223Leu
ENST00000307102.9:c.669C>A ENSP00000302486.4:p.Phe223Leu
ENST00000566326.1:c.141C>A ENSP00000456438.1:p.Phe47Leu
NM_002755.3:c.669C>A , LRG_725t1:c.669C>A NP_002746.1:p.Phe223Leu
XM_011521783.1:c.603C>A XP_011520085.1:p.Phe201Leu
XM_011521783.3:c.603C>A XP_011520085.1:p.Phe201Leu
XM_017022411.2:c.591C>A XP_016877900.1:p.Phe197Leu
XM_017022412.1:c.525C>A XP_016877901.1:p.Phe175Leu
XM_017022413.1:c.141C>A XP_016877902.1:p.Phe47Leu
NM_002755.4:c.669C>A MANE Select NP_002746.1:p.Phe223Leu
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