Canonical Allele Identifier: CA2955275377
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4117456dup , CM000681.2:g.4117456dup GRCh38
NC_000019.9:g.4117454dup , CM000681.1:g.4117454dup GRCh37
NC_000019.8:g.4068454dup NCBI36
NG_007996.1:g.11673dup , LRG_750:g.11673dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.705dup
ENST00000687128.1:n.705dup
ENST00000262948.10:c.266dup MANE Select ENSP00000262948.4:p.Gln90ProfsTer17
ENST00000262948.9:c.266dup ENSP00000262948.3:p.Gln90ProfsTer17
ENST00000394867.8:c.-26dup ENSP00000378336.1:n.-26dup
ENST00000599345.1:n.463dup
NM_030662.3:c.266dup , LRG_750t1:c.266dup NP_109587.1:p.Gln90ProfsTer17
XM_006722799.2:c.266dup XP_006722862.1:p.Gln90ProfsTer17
XM_017026989.1:c.266dup XP_016882478.1:p.Gln90ProfsTer17
XM_017026990.1:c.266dup XP_016882479.1:p.Gln90ProfsTer17
XM_017026991.1:c.266dup XP_016882480.1:p.Gln90ProfsTer17
NM_030662.4:c.266dup MANE Select NP_109587.1:p.Gln90ProfsTer17