Canonical Allele Identifier: CA2184100091
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485135_66485138delinsAAGG , CM000677.2:g.66485135_66485138delinsAAGG GRCh38
NC_000015.9:g.66777473_66777476delinsAAGG , CM000677.1:g.66777473_66777476delinsAAGG GRCh37
NC_000015.8:g.64564527_64564530delinsAAGG NCBI36
NG_008305.1:g.103263_103266delinsAAGG , LRG_725:g.103263_103266delinsAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2093_628-2090delinsAAGG ENSP00000508681.1:n.628-2093_628-2090delinsAAGG
ENST00000685172.1:c.839_842delinsAAGG ENSP00000509604.1:p.Glu280=
ENST00000685763.1:c.692_695delinsAAGG ENSP00000509016.1:p.Glu231=
ENST00000686347.1:c.569-2093_569-2090delinsAAGG ENSP00000509027.1:n.569-2093_569-2090delinsAAGG
ENST00000687191.1:n.1197_1200delinsAAGG
ENST00000687481.1:n.254_257delinsAAGG
ENST00000689951.1:c.890_893delinsAAGG ENSP00000509308.1:p.Glu297=
ENST00000691077.1:c.*76_*79delinsAAGG ENSP00000509843.1:n.*76_*79delinsAAGG
ENST00000691576.1:c.710_713delinsAAGG ENSP00000510066.1:p.Glu237=
ENST00000691937.1:c.839_842delinsAAGG ENSP00000508768.1:p.Glu280=
ENST00000692487.1:c.*76_*79delinsAAGG ENSP00000509534.1:n.*76_*79delinsAAGG
ENST00000692683.1:c.773_776delinsAAGG ENSP00000508437.1:p.Glu258=
ENST00000693150.1:c.695_698delinsAAGG ENSP00000510309.1:p.Glu232=
ENST00000307102.10:c.839_842delinsAAGG MANE Select ENSP00000302486.5:p.Glu280=
ENST00000307102.9:c.839_842delinsAAGG ENSP00000302486.4:p.Glu280=
ENST00000566326.1:c.311_314delinsAAGG ENSP00000456438.1:p.Glu104=
NM_002755.3:c.839_842delinsAAGG , LRG_725t1:c.839_842delinsAAGG NP_002746.1:p.Glu280=
XM_011521783.1:c.773_776delinsAAGG XP_011520085.1:p.Glu258=
XM_011521783.3:c.773_776delinsAAGG XP_011520085.1:p.Glu258=
XM_017022411.2:c.761_764delinsAAGG XP_016877900.1:p.Glu254=
XM_017022412.1:c.695_698delinsAAGG XP_016877901.1:p.Glu232=
XM_017022413.1:c.311_314delinsAAGG XP_016877902.1:p.Glu104=
NM_002755.4:c.839_842delinsAAGG MANE Select NP_002746.1:p.Glu280=