Canonical Allele Identifier: CA490858441
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140668307
MyVariant Identifiers: chr15:g.66774202A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481864A>G , CM000677.2:g.66481864A>G GRCh38
NC_000015.9:g.66774202A>G , CM000677.1:g.66774202A>G GRCh37
NC_000015.8:g.64561256A>G NCBI36
NG_008305.1:g.99992A>G , LRG_725:g.99992A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.612A>G ENSP00000508681.1:p.Thr204=
ENST00000685172.1:c.678A>G ENSP00000509604.1:p.Thr226=
ENST00000685763.1:c.531A>G ENSP00000509016.1:p.Thr177=
ENST00000686347.1:c.569-5364A>G ENSP00000509027.1:n.569-5364A>G
ENST00000687191.1:n.1036A>G
ENST00000689951.1:c.729A>G ENSP00000509308.1:p.Thr243=
ENST00000691077.1:c.678A>G ENSP00000509843.1:p.Thr226=
ENST00000691576.1:c.569-3130A>G ENSP00000510066.1:n.569-3130A>G
ENST00000691937.1:c.678A>G ENSP00000508768.1:p.Thr226=
ENST00000692487.1:c.678A>G ENSP00000509534.1:p.Thr226=
ENST00000692683.1:c.612A>G ENSP00000508437.1:p.Thr204=
ENST00000693150.1:c.534A>G ENSP00000510309.1:p.Thr178=
ENST00000307102.10:c.678A>G MANE Select ENSP00000302486.5:p.Thr226=
ENST00000307102.9:c.678A>G ENSP00000302486.4:p.Thr226=
ENST00000566326.1:c.150A>G ENSP00000456438.1:p.Thr50=
NM_002755.3:c.678A>G , LRG_725t1:c.678A>G NP_002746.1:p.Thr226=
XM_011521783.1:c.612A>G XP_011520085.1:p.Thr204=
XM_011521783.3:c.612A>G XP_011520085.1:p.Thr204=
XM_017022411.2:c.600A>G XP_016877900.1:p.Thr200=
XM_017022412.1:c.534A>G XP_016877901.1:p.Thr178=
XM_017022413.1:c.150A>G XP_016877902.1:p.Thr50=
NM_002755.4:c.678A>G MANE Select NP_002746.1:p.Thr226=
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