Canonical Allele Identifier: CA392936230
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140667617
MyVariant Identifiers: chr15:g.66774138A>T (hg19) chr15:g.66481800A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481800A>T , CM000677.2:g.66481800A>T GRCh38
NC_000015.9:g.66774138A>T , CM000677.1:g.66774138A>T GRCh37
NC_000015.8:g.64561192A>T NCBI36
NG_008305.1:g.99928A>T , LRG_725:g.99928A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.548A>T ENSP00000508681.1:p.Lys183Met
ENST00000685172.1:c.614A>T ENSP00000509604.1:p.Lys205Met
ENST00000685763.1:c.467A>T ENSP00000509016.1:p.Lys156Met
ENST00000686347.1:c.569-5428A>T ENSP00000509027.1:n.569-5428A>T
ENST00000687191.1:n.972A>T
ENST00000689951.1:c.665A>T ENSP00000509308.1:p.Lys222Met
ENST00000691077.1:c.614A>T ENSP00000509843.1:p.Lys205Met
ENST00000691576.1:c.569-3194A>T ENSP00000510066.1:n.569-3194A>T
ENST00000691937.1:c.614A>T ENSP00000508768.1:p.Lys205Met
ENST00000692487.1:c.614A>T ENSP00000509534.1:p.Lys205Met
ENST00000692683.1:c.548A>T ENSP00000508437.1:p.Lys183Met
ENST00000693150.1:c.470A>T ENSP00000510309.1:p.Lys157Met
ENST00000307102.10:c.614A>T MANE Select ENSP00000302486.5:p.Lys205Met
ENST00000307102.9:c.614A>T ENSP00000302486.4:p.Lys205Met
ENST00000566326.1:c.86A>T ENSP00000456438.1:p.Lys29Met
NM_002755.3:c.614A>T , LRG_725t1:c.614A>T NP_002746.1:p.Lys205Met
XM_011521783.1:c.548A>T XP_011520085.1:p.Lys183Met
XM_011521783.3:c.548A>T XP_011520085.1:p.Lys183Met
XM_017022411.2:c.536A>T XP_016877900.1:p.Lys179Met
XM_017022412.1:c.470A>T XP_016877901.1:p.Lys157Met
XM_017022413.1:c.86A>T XP_016877902.1:p.Lys29Met
NM_002755.4:c.614A>T MANE Select NP_002746.1:p.Lys205Met
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