Canonical Allele Identifier: CA2629083704
Gene: MAP2K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485336_66485338dup , CM000677.2:g.66485336_66485338dup GRCh38
NC_000015.9:g.66777674_66777676dup , CM000677.1:g.66777674_66777676dup GRCh37
NC_000015.8:g.64564728_64564730dup NCBI36
NG_008305.1:g.103464_103466dup , LRG_725:g.103464_103466dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-1892_628-1890dup ENSP00000508681.1:n.628-1892_628-1890dup
ENST00000685172.1:c.895+145_895+147dup ENSP00000509604.1:n.895+145_895+147dup
ENST00000685763.1:c.748+145_748+147dup ENSP00000509016.1:n.748+145_748+147dup
ENST00000686347.1:c.569-1892_569-1890dup ENSP00000509027.1:n.569-1892_569-1890dup
ENST00000687191.1:n.1253+145_1253+147dup
ENST00000687481.1:n.310+145_310+147dup
ENST00000689951.1:c.946+145_946+147dup ENSP00000509308.1:n.946+145_946+147dup
ENST00000691077.1:c.*132+145_*132+147dup ENSP00000509843.1:n.*132+145_*132+147dup
ENST00000691576.1:c.766+145_766+147dup ENSP00000510066.1:n.766+145_766+147dup
ENST00000691937.1:c.895+145_895+147dup ENSP00000508768.1:n.895+145_895+147dup
ENST00000692487.1:c.*132+145_*132+147dup ENSP00000509534.1:n.*132+145_*132+147dup
ENST00000692683.1:c.829+145_829+147dup ENSP00000508437.1:n.829+145_829+147dup
ENST00000693150.1:c.751+145_751+147dup ENSP00000510309.1:n.751+145_751+147dup
ENST00000307102.10:c.895+145_895+147dup MANE Select ENSP00000302486.5:n.895+145_895+147dup
ENST00000307102.9:c.895+145_895+147dup ENSP00000302486.4:n.895+145_895+147dup
ENST00000566326.1:c.367+145_367+147dup ENSP00000456438.1:n.367+145_367+147dup
NM_002755.3:c.895+145_895+147dup , LRG_725t1:c.895+145_895+147dup NP_002746.1:n.895+145_895+147dup
XM_011521783.1:c.829+145_829+147dup XP_011520085.1:n.829+145_829+147dup
XM_011521783.3:c.829+145_829+147dup XP_011520085.1:n.829+145_829+147dup
XM_017022411.2:c.817+145_817+147dup XP_016877900.1:n.817+145_817+147dup
XM_017022412.1:c.751+145_751+147dup XP_016877901.1:n.751+145_751+147dup
XM_017022413.1:c.367+145_367+147dup XP_016877902.1:n.367+145_367+147dup
NM_002755.4:c.895+145_895+147dup MANE Select NP_002746.1:n.895+145_895+147dup