Canonical Allele Identifier: CA2184099998
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485026T= , CM000677.2:g.66485026T= GRCh38
NC_000015.9:g.66777364T= , CM000677.1:g.66777364T= GRCh37
NC_000015.8:g.64564418T= NCBI36
NG_008305.1:g.103154T= , LRG_725:g.103154T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2202T= ENSP00000508681.1:n.628-2202T=
ENST00000685172.1:c.730T= ENSP00000509604.1:p.Ser244=
ENST00000685763.1:c.583T= ENSP00000509016.1:p.Ser195=
ENST00000686347.1:c.569-2202T= ENSP00000509027.1:n.569-2202T=
ENST00000687191.1:n.1088T=
ENST00000687481.1:n.145T=
ENST00000689951.1:c.781T= ENSP00000509308.1:p.Ser261=
ENST00000691077.1:c.726T= ENSP00000509843.1:p.Ser242=
ENST00000691576.1:c.601T= ENSP00000510066.1:p.Ser201=
ENST00000691937.1:c.730T= ENSP00000508768.1:p.Ser244=
ENST00000692487.1:c.726T= ENSP00000509534.1:p.Ser242=
ENST00000692683.1:c.664T= ENSP00000508437.1:p.Ser222=
ENST00000693150.1:c.586T= ENSP00000510309.1:p.Ser196=
ENST00000307102.10:c.730T= MANE Select ENSP00000302486.5:p.Ser244=
ENST00000307102.9:c.730T= ENSP00000302486.4:p.Ser244=
ENST00000566326.1:c.202T= ENSP00000456438.1:p.Ser68=
NM_002755.3:c.730T= , LRG_725t1:c.730T= NP_002746.1:p.Ser244=
XM_011521783.1:c.664T= XP_011520085.1:p.Ser222=
XM_011521783.3:c.664T= XP_011520085.1:p.Ser222=
XM_017022411.2:c.652T= XP_016877900.1:p.Ser218=
XM_017022412.1:c.586T= XP_016877901.1:p.Ser196=
XM_017022413.1:c.202T= XP_016877902.1:p.Ser68=
NM_002755.4:c.730T= MANE Select NP_002746.1:p.Ser244=