Canonical Allele Identifier: CA392937353
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs2140675235

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485146G>A , CM000677.2:g.66485146G>A GRCh38
NC_000015.9:g.66777484G>A , CM000677.1:g.66777484G>A GRCh37
NC_000015.8:g.64564538G>A NCBI36
NG_008305.1:g.103274G>A , LRG_725:g.103274G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684779.1:c.628-2082G>A ENSP00000508681.1:n.628-2082G>A
ENST00000685172.1:c.850G>A ENSP00000509604.1:p.Ala284Thr
ENST00000685763.1:c.703G>A ENSP00000509016.1:p.Ala235Thr
ENST00000686347.1:c.569-2082G>A ENSP00000509027.1:n.569-2082G>A
ENST00000687191.1:n.1208G>A
ENST00000687481.1:n.265G>A
ENST00000689951.1:c.901G>A ENSP00000509308.1:p.Ala301Thr
ENST00000691077.1:c.*87G>A ENSP00000509843.1:n.*87G>A
ENST00000691576.1:c.721G>A ENSP00000510066.1:p.Ala241Thr
ENST00000691937.1:c.850G>A ENSP00000508768.1:p.Ala284Thr
ENST00000692487.1:c.*87G>A ENSP00000509534.1:n.*87G>A
ENST00000692683.1:c.784G>A ENSP00000508437.1:p.Ala262Thr
ENST00000693150.1:c.706G>A ENSP00000510309.1:p.Ala236Thr
ENST00000307102.10:c.850G>A MANE Select ENSP00000302486.5:p.Ala284Thr
ENST00000307102.9:c.850G>A ENSP00000302486.4:p.Ala284Thr
ENST00000566326.1:c.322G>A ENSP00000456438.1:p.Ala108Thr
NM_002755.3:c.850G>A , LRG_725t1:c.850G>A NP_002746.1:p.Ala284Thr
XM_011521783.1:c.784G>A XP_011520085.1:p.Ala262Thr
XM_011521783.3:c.784G>A XP_011520085.1:p.Ala262Thr
XM_017022411.2:c.772G>A XP_016877900.1:p.Ala258Thr
XM_017022412.1:c.706G>A XP_016877901.1:p.Ala236Thr
XM_017022413.1:c.322G>A XP_016877902.1:p.Ala108Thr
NM_002755.4:c.850G>A MANE Select NP_002746.1:p.Ala284Thr