Canonical Allele Identifier: CA618673391
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs1424652442

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66436725_66436726del , CM000677.2:g.66436725_66436726del GRCh38
NC_000015.9:g.66729063_66729064del , CM000677.1:g.66729063_66729064del GRCh37
NC_000015.8:g.64516117_64516118del NCBI36
NG_008305.1:g.54853_54854del , LRG_725:g.54853_54854del

Transcript Alleles

HGVS Amino-acid change
ENST00000684779.1:c.226-21_226-20del ENSP00000508681.1:n.226-21_226-20del
ENST00000685172.1:c.292-21_292-20del ENSP00000509604.1:n.292-21_292-20del
ENST00000685763.1:c.291+1488_291+1489del ENSP00000509016.1:n.291+1488_291+1489del
ENST00000686347.1:c.292-21_292-20del ENSP00000509027.1:n.292-21_292-20del
ENST00000687191.1:n.728-21_728-20del
ENST00000689951.1:c.292-21_292-20del ENSP00000509308.1:n.292-21_292-20del
ENST00000691077.1:c.292-21_292-20del ENSP00000509843.1:n.292-21_292-20del
ENST00000691576.1:c.292-21_292-20del ENSP00000510066.1:n.292-21_292-20del
ENST00000691937.1:c.292-21_292-20del ENSP00000508768.1:n.292-21_292-20del
ENST00000692487.1:c.292-21_292-20del ENSP00000509534.1:n.292-21_292-20del
ENST00000692683.1:c.226-21_226-20del ENSP00000508437.1:n.226-21_226-20del
ENST00000693150.1:c.226-21_226-20del ENSP00000510309.1:n.226-21_226-20del
ENST00000307102.10:c.292-21_292-20del MANE Select ENSP00000302486.5:n.292-21_292-20del
ENST00000307102.9:c.292-21_292-20del ENSP00000302486.4:n.292-21_292-20del
ENST00000425818.2:n.803-21_803-20del
NM_002755.3:c.292-21_292-20del , LRG_725t1:c.292-21_292-20del NP_002746.1:n.292-21_292-20del
XM_011521783.1:c.226-21_226-20del XP_011520085.1:n.226-21_226-20del
XM_011521783.3:c.226-21_226-20del XP_011520085.1:n.226-21_226-20del
XM_017022411.2:c.292-21_292-20del XP_016877900.1:n.292-21_292-20del
XM_017022412.1:c.226-21_226-20del XP_016877901.1:n.226-21_226-20del
NM_002755.4:c.292-21_292-20del MANE Select NP_002746.1:n.292-21_292-20del