Canonical Allele Identifier: CA2184100044
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485097T= , CM000677.2:g.66485097T= GRCh38
NC_000015.9:g.66777435T= , CM000677.1:g.66777435T= GRCh37
NC_000015.8:g.64564489T= NCBI36
NG_008305.1:g.103225T= , LRG_725:g.103225T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2131T= ENSP00000508681.1:n.628-2131T=
ENST00000685172.1:c.801T= ENSP00000509604.1:p.Asp267=
ENST00000685763.1:c.654T= ENSP00000509016.1:p.Asp218=
ENST00000686347.1:c.569-2131T= ENSP00000509027.1:n.569-2131T=
ENST00000687191.1:n.1159T=
ENST00000687481.1:n.216T=
ENST00000689951.1:c.852T= ENSP00000509308.1:p.Asp284=
ENST00000691077.1:c.*38T= ENSP00000509843.1:n.*38T=
ENST00000691576.1:c.672T= ENSP00000510066.1:p.Asp224=
ENST00000691937.1:c.801T= ENSP00000508768.1:p.Asp267=
ENST00000692487.1:c.*38T= ENSP00000509534.1:n.*38T=
ENST00000692683.1:c.735T= ENSP00000508437.1:p.Asp245=
ENST00000693150.1:c.657T= ENSP00000510309.1:p.Asp219=
ENST00000307102.10:c.801T= MANE Select ENSP00000302486.5:p.Asp267=
ENST00000307102.9:c.801T= ENSP00000302486.4:p.Asp267=
ENST00000566326.1:c.273T= ENSP00000456438.1:p.Asp91=
NM_002755.3:c.801T= , LRG_725t1:c.801T= NP_002746.1:p.Asp267=
XM_011521783.1:c.735T= XP_011520085.1:p.Asp245=
XM_011521783.3:c.735T= XP_011520085.1:p.Asp245=
XM_017022411.2:c.723T= XP_016877900.1:p.Asp241=
XM_017022412.1:c.657T= XP_016877901.1:p.Asp219=
XM_017022413.1:c.273T= XP_016877902.1:p.Asp91=
NM_002755.4:c.801T= MANE Select NP_002746.1:p.Asp267=