Canonical Allele Identifier: CA2184100054
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485103G= , CM000677.2:g.66485103G= GRCh38
NC_000015.9:g.66777441G= , CM000677.1:g.66777441G= GRCh37
NC_000015.8:g.64564495G= NCBI36
NG_008305.1:g.103231G= , LRG_725:g.103231G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2125G= ENSP00000508681.1:n.628-2125G=
ENST00000685172.1:c.807G= ENSP00000509604.1:p.Lys269=
ENST00000685763.1:c.660G= ENSP00000509016.1:p.Lys220=
ENST00000686347.1:c.569-2125G= ENSP00000509027.1:n.569-2125G=
ENST00000687191.1:n.1165G=
ENST00000687481.1:n.222G=
ENST00000689951.1:c.858G= ENSP00000509308.1:p.Lys286=
ENST00000691077.1:c.*44G= ENSP00000509843.1:n.*44G=
ENST00000691576.1:c.678G= ENSP00000510066.1:p.Lys226=
ENST00000691937.1:c.807G= ENSP00000508768.1:p.Lys269=
ENST00000692487.1:c.*44G= ENSP00000509534.1:n.*44G=
ENST00000692683.1:c.741G= ENSP00000508437.1:p.Lys247=
ENST00000693150.1:c.663G= ENSP00000510309.1:p.Lys221=
ENST00000307102.10:c.807G= MANE Select ENSP00000302486.5:p.Lys269=
ENST00000307102.9:c.807G= ENSP00000302486.4:p.Lys269=
ENST00000566326.1:c.279G= ENSP00000456438.1:p.Lys93=
NM_002755.3:c.807G= , LRG_725t1:c.807G= NP_002746.1:p.Lys269=
XM_011521783.1:c.741G= XP_011520085.1:p.Lys247=
XM_011521783.3:c.741G= XP_011520085.1:p.Lys247=
XM_017022411.2:c.729G= XP_016877900.1:p.Lys243=
XM_017022412.1:c.663G= XP_016877901.1:p.Lys221=
XM_017022413.1:c.279G= XP_016877902.1:p.Lys93=
NM_002755.4:c.807G= MANE Select NP_002746.1:p.Lys269=