Canonical Allele Identifier: CA2184100142
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485171C= , CM000677.2:g.66485171C= GRCh38
NC_000015.9:g.66777509C= , CM000677.1:g.66777509C= GRCh37
NC_000015.8:g.64564563C= NCBI36
NG_008305.1:g.103299C= , LRG_725:g.103299C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2057C= ENSP00000508681.1:n.628-2057C=
ENST00000685172.1:c.875C= ENSP00000509604.1:p.Thr292=
ENST00000685763.1:c.728C= ENSP00000509016.1:p.Thr243=
ENST00000686347.1:c.569-2057C= ENSP00000509027.1:n.569-2057C=
ENST00000687191.1:n.1233C=
ENST00000687481.1:n.290C=
ENST00000689951.1:c.926C= ENSP00000509308.1:p.Thr309=
ENST00000691077.1:c.*112C= ENSP00000509843.1:n.*112C=
ENST00000691576.1:c.746C= ENSP00000510066.1:p.Thr249=
ENST00000691937.1:c.875C= ENSP00000508768.1:p.Thr292=
ENST00000692487.1:c.*112C= ENSP00000509534.1:n.*112C=
ENST00000692683.1:c.809C= ENSP00000508437.1:p.Thr270=
ENST00000693150.1:c.731C= ENSP00000510309.1:p.Thr244=
ENST00000307102.10:c.875C= MANE Select ENSP00000302486.5:p.Thr292=
ENST00000307102.9:c.875C= ENSP00000302486.4:p.Thr292=
ENST00000566326.1:c.347C= ENSP00000456438.1:p.Thr116=
NM_002755.3:c.875C= , LRG_725t1:c.875C= NP_002746.1:p.Thr292=
XM_011521783.1:c.809C= XP_011520085.1:p.Thr270=
XM_011521783.3:c.809C= XP_011520085.1:p.Thr270=
XM_017022411.2:c.797C= XP_016877900.1:p.Thr266=
XM_017022412.1:c.731C= XP_016877901.1:p.Thr244=
XM_017022413.1:c.347C= XP_016877902.1:p.Thr116=
NM_002755.4:c.875C= MANE Select NP_002746.1:p.Thr292=