Canonical Allele Identifier: CA490858439
Gene: MAP2K1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.66774199C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481861C>A , CM000677.2:g.66481861C>A GRCh38
NC_000015.9:g.66774199C>A , CM000677.1:g.66774199C>A GRCh37
NC_000015.8:g.64561253C>A NCBI36
NG_008305.1:g.99989C>A , LRG_725:g.99989C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.609C>A ENSP00000508681.1:p.Gly203=
ENST00000685172.1:c.675C>A ENSP00000509604.1:p.Gly225=
ENST00000685763.1:c.528C>A ENSP00000509016.1:p.Gly176=
ENST00000686347.1:c.569-5367C>A ENSP00000509027.1:n.569-5367C>A
ENST00000687191.1:n.1033C>A
ENST00000689951.1:c.726C>A ENSP00000509308.1:p.Gly242=
ENST00000691077.1:c.675C>A ENSP00000509843.1:p.Gly225=
ENST00000691576.1:c.569-3133C>A ENSP00000510066.1:n.569-3133C>A
ENST00000691937.1:c.675C>A ENSP00000508768.1:p.Gly225=
ENST00000692487.1:c.675C>A ENSP00000509534.1:p.Gly225=
ENST00000692683.1:c.609C>A ENSP00000508437.1:p.Gly203=
ENST00000693150.1:c.531C>A ENSP00000510309.1:p.Gly177=
ENST00000307102.10:c.675C>A MANE Select ENSP00000302486.5:p.Gly225=
ENST00000307102.9:c.675C>A ENSP00000302486.4:p.Gly225=
ENST00000566326.1:c.147C>A ENSP00000456438.1:p.Gly49=
NM_002755.3:c.675C>A , LRG_725t1:c.675C>A NP_002746.1:p.Gly225=
XM_011521783.1:c.609C>A XP_011520085.1:p.Gly203=
XM_011521783.3:c.609C>A XP_011520085.1:p.Gly203=
XM_017022411.2:c.597C>A XP_016877900.1:p.Gly199=
XM_017022412.1:c.531C>A XP_016877901.1:p.Gly177=
XM_017022413.1:c.147C>A XP_016877902.1:p.Gly49=
NM_002755.4:c.675C>A MANE Select NP_002746.1:p.Gly225=
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