Canonical Allele Identifier: CA392936232
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140667617
MyVariant Identifiers: chr15:g.66774138A>G (hg19) chr15:g.66481800A>G (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.548A>G ENSP00000508681.1:p.Lys183Arg
ENST00000685172.1:c.614A>G ENSP00000509604.1:p.Lys205Arg
ENST00000685763.1:c.467A>G ENSP00000509016.1:p.Lys156Arg
ENST00000686347.1:c.569-5428A>G ENSP00000509027.1:n.569-5428A>G
ENST00000687191.1:n.972A>G
ENST00000689951.1:c.665A>G ENSP00000509308.1:p.Lys222Arg
ENST00000691077.1:c.614A>G ENSP00000509843.1:p.Lys205Arg
ENST00000691576.1:c.569-3194A>G ENSP00000510066.1:n.569-3194A>G
ENST00000691937.1:c.614A>G ENSP00000508768.1:p.Lys205Arg
ENST00000692487.1:c.614A>G ENSP00000509534.1:p.Lys205Arg
ENST00000692683.1:c.548A>G ENSP00000508437.1:p.Lys183Arg
ENST00000693150.1:c.470A>G ENSP00000510309.1:p.Lys157Arg
ENST00000307102.10:c.614A>G MANE Select ENSP00000302486.5:p.Lys205Arg
ENST00000307102.9:c.614A>G ENSP00000302486.4:p.Lys205Arg
ENST00000566326.1:c.86A>G ENSP00000456438.1:p.Lys29Arg
NM_002755.3:c.614A>G , LRG_725t1:c.614A>G NP_002746.1:p.Lys205Arg
XM_011521783.1:c.548A>G XP_011520085.1:p.Lys183Arg
XM_011521783.3:c.548A>G XP_011520085.1:p.Lys183Arg
XM_017022411.2:c.536A>G XP_016877900.1:p.Lys179Arg
XM_017022412.1:c.470A>G XP_016877901.1:p.Lys157Arg
XM_017022413.1:c.86A>G XP_016877902.1:p.Lys29Arg
NM_002755.4:c.614A>G MANE Select NP_002746.1:p.Lys205Arg
Search 100 bp 5'
Search 100 bp 3'