Canonical Allele Identifier: CA2319219781
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090682C= , CM000681.2:g.4090682C= GRCh38
NC_000019.9:g.4090680C= , CM000681.1:g.4090680C= GRCh37
NC_000019.8:g.4041680C= NCBI36
NG_007996.1:g.38447G= , LRG_750:g.38447G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1558G=
ENST00000688002.1:n.3270G=
ENST00000688751.1:n.255G=
ENST00000689792.1:n.1023G=
ENST00000262948.10:c.1119G= MANE Select ENSP00000262948.4:p.Glu373=
ENST00000262948.9:c.1119G= ENSP00000262948.3:p.Glu373=
ENST00000394867.8:c.828G= ENSP00000378336.1:p.Glu276=
ENST00000597263.5:n.304G=
ENST00000599021.1:c.229G=
ENST00000600584.5:n.2568G=
ENST00000601786.5:n.1420G=
NM_030662.3:c.1119G= , LRG_750t1:c.1119G= NP_109587.1:p.Glu373=
XM_006722799.2:c.840G= XP_006722862.1:p.Glu280=
XM_011528133.1:c.549G= XP_011526435.1:p.Glu183=
NM_030662.4:c.1119G= MANE Select NP_109587.1:p.Glu373=