Canonical Allele Identifier: CA2804537030
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485164_66485165insACACCCAACA , CM000677.2:g.66485164_66485165insACACCCAACA GRCh38
NC_000015.9:g.66777502_66777503insACACCCAACA , CM000677.1:g.66777502_66777503insACACCCAACA GRCh37
NC_000015.8:g.64564556_64564557insACACCCAACA NCBI36
NG_008305.1:g.103292_103293insACACCCAACA , LRG_725:g.103292_103293insACACCCAACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-2064_628-2063insACACCCAACA ENSP00000508681.1:n.628-2064_628-2063insACACCCAACA
ENST00000685172.1:c.868_869insACACCCAACA ENSP00000509604.1:p.Pro290HisfsTer12
ENST00000685763.1:c.721_722insACACCCAACA ENSP00000509016.1:p.Pro241HisfsTer12
ENST00000686347.1:c.569-2064_569-2063insACACCCAACA ENSP00000509027.1:n.569-2064_569-2063insACACCCAACA
ENST00000687191.1:n.1226_1227insACACCCAACA
ENST00000687481.1:n.283_284insACACCCAACA
ENST00000689951.1:c.919_920insACACCCAACA ENSP00000509308.1:p.Pro307HisfsTer12
ENST00000691077.1:c.*105_*106insACACCCAACA ENSP00000509843.1:n.*105_*106insACACCCAACA
ENST00000691576.1:c.739_740insACACCCAACA ENSP00000510066.1:p.Pro247HisfsTer12
ENST00000691937.1:c.868_869insACACCCAACA ENSP00000508768.1:p.Pro290HisfsTer12
ENST00000692487.1:c.*105_*106insACACCCAACA ENSP00000509534.1:n.*105_*106insACACCCAACA
ENST00000692683.1:c.802_803insACACCCAACA ENSP00000508437.1:p.Pro268HisfsTer12
ENST00000693150.1:c.724_725insACACCCAACA ENSP00000510309.1:p.Pro242HisfsTer12
ENST00000307102.10:c.868_869insACACCCAACA MANE Select ENSP00000302486.5:p.Pro290HisfsTer12
ENST00000307102.9:c.868_869insACACCCAACA ENSP00000302486.4:p.Pro290HisfsTer12
ENST00000566326.1:c.340_341insACACCCAACA ENSP00000456438.1:p.Pro114HisfsTer12
NM_002755.3:c.868_869insACACCCAACA , LRG_725t1:c.868_869insACACCCAACA NP_002746.1:p.Pro290HisfsTer12
XM_011521783.1:c.802_803insACACCCAACA XP_011520085.1:p.Pro268HisfsTer12
XM_011521783.3:c.802_803insACACCCAACA XP_011520085.1:p.Pro268HisfsTer12
XM_017022411.2:c.790_791insACACCCAACA XP_016877900.1:p.Pro264HisfsTer12
XM_017022412.1:c.724_725insACACCCAACA XP_016877901.1:p.Pro242HisfsTer12
XM_017022413.1:c.340_341insACACCCAACA XP_016877902.1:p.Pro114HisfsTer12
NM_002755.4:c.868_869insACACCCAACA MANE Select NP_002746.1:p.Pro290HisfsTer12