Canonical Allele Identifier: CA392936335
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs1313264011
MyVariant Identifiers: chr15:g.66774161G>C (hg19) chr15:g.66481823G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481823G>C , CM000677.2:g.66481823G>C GRCh38
NC_000015.9:g.66774161G>C , CM000677.1:g.66774161G>C GRCh37
NC_000015.8:g.64561215G>C NCBI36
NG_008305.1:g.99951G>C , LRG_725:g.99951G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.571G>C ENSP00000508681.1:p.Gly191Arg
ENST00000685172.1:c.637G>C ENSP00000509604.1:p.Gly213Arg
ENST00000685763.1:c.490G>C ENSP00000509016.1:p.Gly164Arg
ENST00000686347.1:c.569-5405G>C ENSP00000509027.1:n.569-5405G>C
ENST00000687191.1:n.995G>C
ENST00000689951.1:c.688G>C ENSP00000509308.1:p.Gly230Arg
ENST00000691077.1:c.637G>C ENSP00000509843.1:p.Gly213Arg
ENST00000691576.1:c.569-3171G>C ENSP00000510066.1:n.569-3171G>C
ENST00000691937.1:c.637G>C ENSP00000508768.1:p.Gly213Arg
ENST00000692487.1:c.637G>C ENSP00000509534.1:p.Gly213Arg
ENST00000692683.1:c.571G>C ENSP00000508437.1:p.Gly191Arg
ENST00000693150.1:c.493G>C ENSP00000510309.1:p.Gly165Arg
ENST00000307102.10:c.637G>C MANE Select ENSP00000302486.5:p.Gly213Arg
ENST00000307102.9:c.637G>C ENSP00000302486.4:p.Gly213Arg
ENST00000566326.1:c.109G>C ENSP00000456438.1:p.Gly37Arg
NM_002755.3:c.637G>C , LRG_725t1:c.637G>C NP_002746.1:p.Gly213Arg
XM_011521783.1:c.571G>C XP_011520085.1:p.Gly191Arg
XM_011521783.3:c.571G>C XP_011520085.1:p.Gly191Arg
XM_017022411.2:c.559G>C XP_016877900.1:p.Gly187Arg
XM_017022412.1:c.493G>C XP_016877901.1:p.Gly165Arg
XM_017022413.1:c.109G>C XP_016877902.1:p.Gly37Arg
NM_002755.4:c.637G>C MANE Select NP_002746.1:p.Gly213Arg
Search 100 bp 5'
Search 100 bp 3'