Canonical Allele Identifier: CA2319224432

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099345C= , CM000681.2:g.4099345C=	GRCh38
NC_000019.9:g.4099343C= , CM000681.1:g.4099343C=	GRCh37
NC_000019.8:g.4050343C=	NCBI36
NG_007996.1:g.29784G= , LRG_750:g.29784G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1214G=
ENST00000687128.1:n.1214G=
ENST00000688002.1:n.1069G=
ENST00000689792.1:n.679G=
ENST00000262948.10:c.775G= MANE Select	ENSP00000262948.4:p.Glu259=
ENST00000262948.9:c.775G=	ENSP00000262948.3:p.Glu259=
ENST00000394867.8:c.484G=	ENSP00000378336.1:p.Glu162=
ENST00000593364.5:n.722G=
ENST00000595715.1:n.590G=
ENST00000597263.5:n.169+1674G=
ENST00000599021.1:c.29+1674G=
ENST00000600584.5:n.1335G=
ENST00000601786.5:n.1076G=
NM_030662.3:c.775G= , LRG_750t1:c.775G=	NP_109587.1:p.Glu259=
XM_006722799.2:c.705+1674G=	XP_006722862.1:n.705+1674G=
XM_011528133.1:c.205G=	XP_011526435.1:p.Glu69=
XM_017026989.1:c.775G=	XP_016882478.1:p.Glu259=
XM_017026990.1:c.705+1674G=	XP_016882479.1:n.705+1674G=
NM_030662.4:c.775G= MANE Select	NP_109587.1:p.Glu259=