Canonical Allele Identifier: CA490858556
Gene: MAP2K1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.66777489G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485151G>A , CM000677.2:g.66485151G>A GRCh38
NC_000015.9:g.66777489G>A , CM000677.1:g.66777489G>A GRCh37
NC_000015.8:g.64564543G>A NCBI36
NG_008305.1:g.103279G>A , LRG_725:g.103279G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684779.1:c.628-2077G>A ENSP00000508681.1:n.628-2077G>A
ENST00000685172.1:c.855G>A ENSP00000509604.1:p.Glu285=
ENST00000685763.1:c.708G>A ENSP00000509016.1:p.Glu236=
ENST00000686347.1:c.569-2077G>A ENSP00000509027.1:n.569-2077G>A
ENST00000687191.1:n.1213G>A
ENST00000687481.1:n.270G>A
ENST00000689951.1:c.906G>A ENSP00000509308.1:p.Glu302=
ENST00000691077.1:c.*92G>A ENSP00000509843.1:n.*92G>A
ENST00000691576.1:c.726G>A ENSP00000510066.1:p.Glu242=
ENST00000691937.1:c.855G>A ENSP00000508768.1:p.Glu285=
ENST00000692487.1:c.*92G>A ENSP00000509534.1:n.*92G>A
ENST00000692683.1:c.789G>A ENSP00000508437.1:p.Glu263=
ENST00000693150.1:c.711G>A ENSP00000510309.1:p.Glu237=
ENST00000307102.10:c.855G>A MANE Select ENSP00000302486.5:p.Glu285=
ENST00000307102.9:c.855G>A ENSP00000302486.4:p.Glu285=
ENST00000566326.1:c.327G>A ENSP00000456438.1:p.Glu109=
NM_002755.3:c.855G>A , LRG_725t1:c.855G>A NP_002746.1:p.Glu285=
XM_011521783.1:c.789G>A XP_011520085.1:p.Glu263=
XM_011521783.3:c.789G>A XP_011520085.1:p.Glu263=
XM_017022411.2:c.777G>A XP_016877900.1:p.Glu259=
XM_017022412.1:c.711G>A XP_016877901.1:p.Glu237=
XM_017022413.1:c.327G>A XP_016877902.1:p.Glu109=
NM_002755.4:c.855G>A MANE Select NP_002746.1:p.Glu285=
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