Canonical Allele Identifier: CA2766290578
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481843_66481844delinsAA , CM000677.2:g.66481843_66481844delinsAA GRCh38
NC_000015.9:g.66774181_66774182delinsAA , CM000677.1:g.66774181_66774182delinsAA GRCh37
NC_000015.8:g.64561235_64561236delinsAA NCBI36
NG_008305.1:g.99971_99972delinsAA , LRG_725:g.99971_99972delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.591_592delinsAA ENSP00000508681.1:p.Met197_Ala198delinsIleThr
ENST00000685172.1:c.657_658delinsAA ENSP00000509604.1:p.Met219_Ala220delinsIleThr
ENST00000685763.1:c.510_511delinsAA ENSP00000509016.1:p.Met170_Ala171delinsIleThr
ENST00000686347.1:c.569-5385_569-5384delinsAA ENSP00000509027.1:n.569-5385_569-5384delinsAA
ENST00000687191.1:n.1015_1016delinsAA
ENST00000689951.1:c.708_709delinsAA ENSP00000509308.1:p.Met236_Ala237delinsIleThr
ENST00000691077.1:c.657_658delinsAA ENSP00000509843.1:p.Met219_Ala220delinsIleThr
ENST00000691576.1:c.569-3151_569-3150delinsAA ENSP00000510066.1:n.569-3151_569-3150delinsAA
ENST00000691937.1:c.657_658delinsAA ENSP00000508768.1:p.Met219_Ala220delinsIleThr
ENST00000692487.1:c.657_658delinsAA ENSP00000509534.1:p.Met219_Ala220delinsIleThr
ENST00000692683.1:c.591_592delinsAA ENSP00000508437.1:p.Met197_Ala198delinsIleThr
ENST00000693150.1:c.513_514delinsAA ENSP00000510309.1:p.Met171_Ala172delinsIleThr
ENST00000307102.10:c.657_658delinsAA MANE Select ENSP00000302486.5:p.Met219_Ala220delinsIleThr
ENST00000307102.9:c.657_658delinsAA ENSP00000302486.4:p.Met219_Ala220delinsIleThr
ENST00000566326.1:c.129_130delinsAA ENSP00000456438.1:p.Met43_Ala44delinsIleThr
NM_002755.3:c.657_658delinsAA , LRG_725t1:c.657_658delinsAA NP_002746.1:p.Met219_Ala220delinsIleThr
XM_011521783.1:c.591_592delinsAA XP_011520085.1:p.Met197_Ala198delinsIleThr
XM_011521783.3:c.591_592delinsAA XP_011520085.1:p.Met197_Ala198delinsIleThr
XM_017022411.2:c.579_580delinsAA XP_016877900.1:p.Met193_Ala194delinsIleThr
XM_017022412.1:c.513_514delinsAA XP_016877901.1:p.Met171_Ala172delinsIleThr
XM_017022413.1:c.129_130delinsAA XP_016877902.1:p.Met43_Ala44delinsIleThr
NM_002755.4:c.657_658delinsAA MANE Select NP_002746.1:p.Met219_Ala220delinsIleThr