Canonical Allele Identifier: CA392936955
Gene: MAP2K1 HGNC NCBI

Linked Data

COSMIC: COSM964226
MyVariant Identifiers: chr15:g.66777356C>A (hg19) chr15:g.66485018C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485018C>A , CM000677.2:g.66485018C>A GRCh38
NC_000015.9:g.66777356C>A , CM000677.1:g.66777356C>A GRCh37
NC_000015.8:g.64564410C>A NCBI36
NG_008305.1:g.103146C>A , LRG_725:g.103146C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2210C>A ENSP00000508681.1:n.628-2210C>A
ENST00000685172.1:c.722C>A ENSP00000509604.1:p.Ser241Tyr
ENST00000685763.1:c.575C>A ENSP00000509016.1:p.Ser192Tyr
ENST00000686347.1:c.569-2210C>A ENSP00000509027.1:n.569-2210C>A
ENST00000687191.1:n.1080C>A
ENST00000687481.1:n.137C>A
ENST00000689951.1:c.773C>A ENSP00000509308.1:p.Ser258Tyr
ENST00000691077.1:c.718C>A ENSP00000509843.1:p.Leu240Met
ENST00000691576.1:c.593C>A ENSP00000510066.1:p.Ser198Tyr
ENST00000691937.1:c.722C>A ENSP00000508768.1:p.Ser241Tyr
ENST00000692487.1:c.718C>A ENSP00000509534.1:p.Leu240Met
ENST00000692683.1:c.656C>A ENSP00000508437.1:p.Ser219Tyr
ENST00000693150.1:c.578C>A ENSP00000510309.1:p.Ser193Tyr
ENST00000307102.10:c.722C>A MANE Select ENSP00000302486.5:p.Ser241Tyr
ENST00000307102.9:c.722C>A ENSP00000302486.4:p.Ser241Tyr
ENST00000566326.1:c.194C>A ENSP00000456438.1:p.Ser65Tyr
NM_002755.3:c.722C>A , LRG_725t1:c.722C>A NP_002746.1:p.Ser241Tyr
XM_011521783.1:c.656C>A XP_011520085.1:p.Ser219Tyr
XM_011521783.3:c.656C>A XP_011520085.1:p.Ser219Tyr
XM_017022411.2:c.644C>A XP_016877900.1:p.Ser215Tyr
XM_017022412.1:c.578C>A XP_016877901.1:p.Ser193Tyr
XM_017022413.1:c.194C>A XP_016877902.1:p.Ser65Tyr
NM_002755.4:c.722C>A MANE Select NP_002746.1:p.Ser241Tyr
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