Canonical Allele Identifier: CA2184100371
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485440_66485441delinsAC , CM000677.2:g.66485440_66485441delinsAC GRCh38
NC_000015.9:g.66777778_66777779delinsAC , CM000677.1:g.66777778_66777779delinsAC GRCh37
NC_000015.8:g.64564832_64564833delinsAC NCBI36
NG_008305.1:g.103568_103569delinsAC , LRG_725:g.103568_103569delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-1788_628-1787delinsAC ENSP00000508681.1:n.628-1788_628-1787delinsAC
ENST00000685172.1:c.895+249_895+250delinsAC ENSP00000509604.1:n.895+249_895+250delinsAC
ENST00000685763.1:c.748+249_748+250delinsAC ENSP00000509016.1:n.748+249_748+250delinsAC
ENST00000686347.1:c.569-1788_569-1787delinsAC ENSP00000509027.1:n.569-1788_569-1787delinsAC
ENST00000687191.1:n.1253+249_1253+250delinsAC
ENST00000687481.1:n.310+249_310+250delinsAC
ENST00000689951.1:c.946+249_946+250delinsAC ENSP00000509308.1:n.946+249_946+250delinsAC
ENST00000691077.1:c.*132+249_*132+250delinsAC ENSP00000509843.1:n.*132+249_*132+250delinsAC
ENST00000691576.1:c.766+249_766+250delinsAC ENSP00000510066.1:n.766+249_766+250delinsAC
ENST00000691937.1:c.895+249_895+250delinsAC ENSP00000508768.1:n.895+249_895+250delinsAC
ENST00000692487.1:c.*132+249_*132+250delinsAC ENSP00000509534.1:n.*132+249_*132+250delinsAC
ENST00000692683.1:c.829+249_829+250delinsAC ENSP00000508437.1:n.829+249_829+250delinsAC
ENST00000693150.1:c.751+249_751+250delinsAC ENSP00000510309.1:n.751+249_751+250delinsAC
ENST00000307102.10:c.895+249_895+250delinsAC MANE Select ENSP00000302486.5:n.895+249_895+250delinsAC
ENST00000307102.9:c.895+249_895+250delinsAC ENSP00000302486.4:n.895+249_895+250delinsAC
ENST00000566326.1:c.367+249_367+250delinsAC ENSP00000456438.1:n.367+249_367+250delinsAC
NM_002755.3:c.895+249_895+250delinsAC , LRG_725t1:c.895+249_895+250delinsAC NP_002746.1:n.895+249_895+250delinsAC
XM_011521783.1:c.829+249_829+250delinsAC XP_011520085.1:n.829+249_829+250delinsAC
XM_011521783.3:c.829+249_829+250delinsAC XP_011520085.1:n.829+249_829+250delinsAC
XM_017022411.2:c.817+249_817+250delinsAC XP_016877900.1:n.817+249_817+250delinsAC
XM_017022412.1:c.751+249_751+250delinsAC XP_016877901.1:n.751+249_751+250delinsAC
XM_017022413.1:c.367+249_367+250delinsAC XP_016877902.1:n.367+249_367+250delinsAC
NM_002755.4:c.895+249_895+250delinsAC MANE Select NP_002746.1:n.895+249_895+250delinsAC