Canonical Allele Identifier: CA2184099987
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485016C= , CM000677.2:g.66485016C= GRCh38
NC_000015.9:g.66777354C= , CM000677.1:g.66777354C= GRCh37
NC_000015.8:g.64564408C= NCBI36
NG_008305.1:g.103144C= , LRG_725:g.103144C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2212C= ENSP00000508681.1:n.628-2212C=
ENST00000685172.1:c.720C= ENSP00000509604.1:p.Tyr240=
ENST00000685763.1:c.573C= ENSP00000509016.1:p.Tyr191=
ENST00000686347.1:c.569-2212C= ENSP00000509027.1:n.569-2212C=
ENST00000687191.1:n.1078C=
ENST00000687481.1:n.135C=
ENST00000689951.1:c.771C= ENSP00000509308.1:p.Tyr257=
ENST00000691077.1:c.716C= ENSP00000509843.1:p.Thr239=
ENST00000691576.1:c.591C= ENSP00000510066.1:p.Tyr197=
ENST00000691937.1:c.720C= ENSP00000508768.1:p.Tyr240=
ENST00000692487.1:c.716C= ENSP00000509534.1:p.Thr239=
ENST00000692683.1:c.654C= ENSP00000508437.1:p.Tyr218=
ENST00000693150.1:c.576C= ENSP00000510309.1:p.Tyr192=
ENST00000307102.10:c.720C= MANE Select ENSP00000302486.5:p.Tyr240=
ENST00000307102.9:c.720C= ENSP00000302486.4:p.Tyr240=
ENST00000566326.1:c.192C= ENSP00000456438.1:p.Tyr64=
NM_002755.3:c.720C= , LRG_725t1:c.720C= NP_002746.1:p.Tyr240=
XM_011521783.1:c.654C= XP_011520085.1:p.Tyr218=
XM_011521783.3:c.654C= XP_011520085.1:p.Tyr218=
XM_017022411.2:c.642C= XP_016877900.1:p.Tyr214=
XM_017022412.1:c.576C= XP_016877901.1:p.Tyr192=
XM_017022413.1:c.192C= XP_016877902.1:p.Tyr64=
NM_002755.4:c.720C= MANE Select NP_002746.1:p.Tyr240=