Canonical Allele Identifier: CA2184100262
Gene: MAP2K1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485313C= , CM000677.2:g.66485313C= GRCh38
NC_000015.9:g.66777651C= , CM000677.1:g.66777651C= GRCh37
NC_000015.8:g.64564705C= NCBI36
NG_008305.1:g.103441C= , LRG_725:g.103441C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-1915C= ENSP00000508681.1:n.628-1915C=
ENST00000685172.1:c.895+122C= ENSP00000509604.1:n.895+122C=
ENST00000685763.1:c.748+122C= ENSP00000509016.1:n.748+122C=
ENST00000686347.1:c.569-1915C= ENSP00000509027.1:n.569-1915C=
ENST00000687191.1:n.1253+122C=
ENST00000687481.1:n.310+122C=
ENST00000689951.1:c.946+122C= ENSP00000509308.1:n.946+122C=
ENST00000691077.1:c.*132+122C= ENSP00000509843.1:n.*132+122C=
ENST00000691576.1:c.766+122C= ENSP00000510066.1:n.766+122C=
ENST00000691937.1:c.895+122C= ENSP00000508768.1:n.895+122C=
ENST00000692487.1:c.*132+122C= ENSP00000509534.1:n.*132+122C=
ENST00000692683.1:c.829+122C= ENSP00000508437.1:n.829+122C=
ENST00000693150.1:c.751+122C= ENSP00000510309.1:n.751+122C=
ENST00000307102.10:c.895+122C= MANE Select ENSP00000302486.5:n.895+122C=
ENST00000307102.9:c.895+122C= ENSP00000302486.4:n.895+122C=
ENST00000566326.1:c.367+122C= ENSP00000456438.1:n.367+122C=
NM_002755.3:c.895+122C= , LRG_725t1:c.895+122C= NP_002746.1:n.895+122C=
XM_011521783.1:c.829+122C= XP_011520085.1:n.829+122C=
XM_011521783.3:c.829+122C= XP_011520085.1:n.829+122C=
XM_017022411.2:c.817+122C= XP_016877900.1:n.817+122C=
XM_017022412.1:c.751+122C= XP_016877901.1:n.751+122C=
XM_017022413.1:c.367+122C= XP_016877902.1:n.367+122C=
NM_002755.4:c.895+122C= MANE Select NP_002746.1:n.895+122C=
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