Canonical Allele Identifier: CA2955275374
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4117455dup , CM000681.2:g.4117455dup GRCh38
NC_000019.9:g.4117453dup , CM000681.1:g.4117453dup GRCh37
NC_000019.8:g.4068453dup NCBI36
NG_007996.1:g.11675dup , LRG_750:g.11675dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.707dup
ENST00000687128.1:n.707dup
ENST00000262948.10:c.268dup MANE Select ENSP00000262948.4:p.Gln90ProfsTer17
ENST00000262948.9:c.268dup ENSP00000262948.3:p.Gln90ProfsTer17
ENST00000394867.8:c.-24dup ENSP00000378336.1:n.-24dup
ENST00000599345.1:n.465dup
NM_030662.3:c.268dup , LRG_750t1:c.268dup NP_109587.1:p.Gln90ProfsTer17
XM_006722799.2:c.268dup XP_006722862.1:p.Gln90ProfsTer17
XM_017026989.1:c.268dup XP_016882478.1:p.Gln90ProfsTer17
XM_017026990.1:c.268dup XP_016882479.1:p.Gln90ProfsTer17
XM_017026991.1:c.268dup XP_016882480.1:p.Gln90ProfsTer17
NM_030662.4:c.268dup MANE Select NP_109587.1:p.Gln90ProfsTer17