Canonical Allele Identifier: CA490858486
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140674218
MyVariant Identifiers: chr15:g.66777384A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485046A>G , CM000677.2:g.66485046A>G GRCh38
NC_000015.9:g.66777384A>G , CM000677.1:g.66777384A>G GRCh37
NC_000015.8:g.64564438A>G NCBI36
NG_008305.1:g.103174A>G , LRG_725:g.103174A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000684779.1:c.628-2182A>G ENSP00000508681.1:n.628-2182A>G
ENST00000685172.1:c.750A>G ENSP00000509604.1:p.Gly250=
ENST00000685763.1:c.603A>G ENSP00000509016.1:p.Gly201=
ENST00000686347.1:c.569-2182A>G ENSP00000509027.1:n.569-2182A>G
ENST00000687191.1:n.1108A>G
ENST00000687481.1:n.165A>G
ENST00000689951.1:c.801A>G ENSP00000509308.1:p.Gly267=
ENST00000691077.1:c.746A>G ENSP00000509843.1:p.Asp249Gly
ENST00000691576.1:c.621A>G ENSP00000510066.1:p.Gly207=
ENST00000691937.1:c.750A>G ENSP00000508768.1:p.Gly250=
ENST00000692487.1:c.746A>G ENSP00000509534.1:p.Asp249Gly
ENST00000692683.1:c.684A>G ENSP00000508437.1:p.Gly228=
ENST00000693150.1:c.606A>G ENSP00000510309.1:p.Gly202=
ENST00000307102.10:c.750A>G MANE Select ENSP00000302486.5:p.Gly250=
ENST00000307102.9:c.750A>G ENSP00000302486.4:p.Gly250=
ENST00000566326.1:c.222A>G ENSP00000456438.1:p.Gly74=
NM_002755.3:c.750A>G , LRG_725t1:c.750A>G NP_002746.1:p.Gly250=
XM_011521783.1:c.684A>G XP_011520085.1:p.Gly228=
XM_011521783.3:c.684A>G XP_011520085.1:p.Gly228=
XM_017022411.2:c.672A>G XP_016877900.1:p.Gly224=
XM_017022412.1:c.606A>G XP_016877901.1:p.Gly202=
XM_017022413.1:c.222A>G XP_016877902.1:p.Gly74=
NM_002755.4:c.750A>G MANE Select NP_002746.1:p.Gly250=
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