Canonical Allele Identifier: CA490858383
Gene: MAP2K1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.66774106C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481768C>A , CM000677.2:g.66481768C>A GRCh38
NC_000015.9:g.66774106C>A , CM000677.1:g.66774106C>A GRCh37
NC_000015.8:g.64561160C>A NCBI36
NG_008305.1:g.99896C>A , LRG_725:g.99896C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.516C>A ENSP00000508681.1:p.Ser172=
ENST00000685172.1:c.582C>A ENSP00000509604.1:p.Ser194=
ENST00000685763.1:c.435C>A ENSP00000509016.1:p.Ser145=
ENST00000686347.1:c.569-5460C>A ENSP00000509027.1:n.569-5460C>A
ENST00000687191.1:n.940C>A
ENST00000689951.1:c.633C>A ENSP00000509308.1:p.Ser211=
ENST00000691077.1:c.582C>A ENSP00000509843.1:p.Ser194=
ENST00000691576.1:c.569-3226C>A ENSP00000510066.1:n.569-3226C>A
ENST00000691937.1:c.582C>A ENSP00000508768.1:p.Ser194=
ENST00000692487.1:c.582C>A ENSP00000509534.1:p.Ser194=
ENST00000692683.1:c.516C>A ENSP00000508437.1:p.Ser172=
ENST00000693150.1:c.438C>A ENSP00000510309.1:p.Ser146=
ENST00000307102.10:c.582C>A MANE Select ENSP00000302486.5:p.Ser194=
ENST00000307102.9:c.582C>A ENSP00000302486.4:p.Ser194=
ENST00000566326.1:c.54C>A ENSP00000456438.1:p.Ser18=
NM_002755.3:c.582C>A , LRG_725t1:c.582C>A NP_002746.1:p.Ser194=
XM_011521783.1:c.516C>A XP_011520085.1:p.Ser172=
XM_011521783.3:c.516C>A XP_011520085.1:p.Ser172=
XM_017022411.2:c.504C>A XP_016877900.1:p.Ser168=
XM_017022412.1:c.438C>A XP_016877901.1:p.Ser146=
XM_017022413.1:c.54C>A XP_016877902.1:p.Ser18=
NM_002755.4:c.582C>A MANE Select NP_002746.1:p.Ser194=