Canonical Allele Identifier: CA392936994
Gene: MAP2K1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.66777374G>T (hg19) chr15:g.66485036G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485036G>T , CM000677.2:g.66485036G>T GRCh38
NC_000015.9:g.66777374G>T , CM000677.1:g.66777374G>T GRCh37
NC_000015.8:g.64564428G>T NCBI36
NG_008305.1:g.103164G>T , LRG_725:g.103164G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2192G>T ENSP00000508681.1:n.628-2192G>T
ENST00000685172.1:c.740G>T ENSP00000509604.1:p.Trp247Leu
ENST00000685763.1:c.593G>T ENSP00000509016.1:p.Trp198Leu
ENST00000686347.1:c.569-2192G>T ENSP00000509027.1:n.569-2192G>T
ENST00000687191.1:n.1098G>T
ENST00000687481.1:n.155G>T
ENST00000689951.1:c.791G>T ENSP00000509308.1:p.Trp264Leu
ENST00000691077.1:c.736G>T ENSP00000509843.1:p.Gly246Ter
ENST00000691576.1:c.611G>T ENSP00000510066.1:p.Trp204Leu
ENST00000691937.1:c.740G>T ENSP00000508768.1:p.Trp247Leu
ENST00000692487.1:c.736G>T ENSP00000509534.1:p.Gly246Ter
ENST00000692683.1:c.674G>T ENSP00000508437.1:p.Trp225Leu
ENST00000693150.1:c.596G>T ENSP00000510309.1:p.Trp199Leu
ENST00000307102.10:c.740G>T MANE Select ENSP00000302486.5:p.Trp247Leu
ENST00000307102.9:c.740G>T ENSP00000302486.4:p.Trp247Leu
ENST00000566326.1:c.212G>T ENSP00000456438.1:p.Trp71Leu
NM_002755.3:c.740G>T , LRG_725t1:c.740G>T NP_002746.1:p.Trp247Leu
XM_011521783.1:c.674G>T XP_011520085.1:p.Trp225Leu
XM_011521783.3:c.674G>T XP_011520085.1:p.Trp225Leu
XM_017022411.2:c.662G>T XP_016877900.1:p.Trp221Leu
XM_017022412.1:c.596G>T XP_016877901.1:p.Trp199Leu
XM_017022413.1:c.212G>T XP_016877902.1:p.Trp71Leu
NM_002755.4:c.740G>T MANE Select NP_002746.1:p.Trp247Leu
Search 100 bp 5'
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