Canonical Allele Identifier: CA715036328
Gene: MAP2K1 HGNC NCBI

Linked Data

dbSNP Id: rs1373256304

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485430_66485436del , CM000677.2:g.66485430_66485436del GRCh38
NC_000015.9:g.66777768_66777774del , CM000677.1:g.66777768_66777774del GRCh37
NC_000015.8:g.64564822_64564828del NCBI36
NG_008305.1:g.103558_103564del , LRG_725:g.103558_103564del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-1798_628-1792del ENSP00000508681.1:n.628-1798_628-1792del
ENST00000685172.1:c.895+239_895+245del ENSP00000509604.1:n.895+239_895+245del
ENST00000685763.1:c.748+239_748+245del ENSP00000509016.1:n.748+239_748+245del
ENST00000686347.1:c.569-1798_569-1792del ENSP00000509027.1:n.569-1798_569-1792del
ENST00000687191.1:n.1253+239_1253+245del
ENST00000687481.1:n.310+239_310+245del
ENST00000689951.1:c.946+239_946+245del ENSP00000509308.1:n.946+239_946+245del
ENST00000691077.1:c.*132+239_*132+245del ENSP00000509843.1:n.*132+239_*132+245del
ENST00000691576.1:c.766+239_766+245del ENSP00000510066.1:n.766+239_766+245del
ENST00000691937.1:c.895+239_895+245del ENSP00000508768.1:n.895+239_895+245del
ENST00000692487.1:c.*132+239_*132+245del ENSP00000509534.1:n.*132+239_*132+245del
ENST00000692683.1:c.829+239_829+245del ENSP00000508437.1:n.829+239_829+245del
ENST00000693150.1:c.751+239_751+245del ENSP00000510309.1:n.751+239_751+245del
ENST00000307102.10:c.895+239_895+245del MANE Select ENSP00000302486.5:n.895+239_895+245del
ENST00000307102.9:c.895+239_895+245del ENSP00000302486.4:n.895+239_895+245del
ENST00000566326.1:c.367+239_367+245del ENSP00000456438.1:n.367+239_367+245del
NM_002755.3:c.895+239_895+245del , LRG_725t1:c.895+239_895+245del NP_002746.1:n.895+239_895+245del
XM_011521783.1:c.829+239_829+245del XP_011520085.1:n.829+239_829+245del
XM_011521783.3:c.829+239_829+245del XP_011520085.1:n.829+239_829+245del
XM_017022411.2:c.817+239_817+245del XP_016877900.1:n.817+239_817+245del
XM_017022412.1:c.751+239_751+245del XP_016877901.1:n.751+239_751+245del
XM_017022413.1:c.367+239_367+245del XP_016877902.1:n.367+239_367+245del
NM_002755.4:c.895+239_895+245del MANE Select NP_002746.1:n.895+239_895+245del