Canonical Allele Identifier: CA2319222239

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095403T= , CM000681.2:g.4095403T=	GRCh38
NC_000019.9:g.4095401T= , CM000681.1:g.4095401T=	GRCh37
NC_000019.8:g.4046401T=	NCBI36
NG_007996.1:g.33726A= , LRG_750:g.33726A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1470A=
ENST00000688002.1:n.3182A=
ENST00000688751.1:n.167A=
ENST00000689792.1:n.935A=
ENST00000262948.10:c.1031A= MANE Select	ENSP00000262948.4:p.Glu344=
ENST00000262948.9:c.1031A=	ENSP00000262948.3:p.Glu344=
ENST00000394867.8:c.740A=	ENSP00000378336.1:p.Glu247=
ENST00000595715.1:n.846A=
ENST00000597263.5:n.216A=
ENST00000599021.1:c.141A=
ENST00000600584.5:n.1591A=
ENST00000601786.5:n.1332A=
NM_030662.3:c.1031A= , LRG_750t1:c.1031A=	NP_109587.1:p.Glu344=
XM_006722799.2:c.752A=	XP_006722862.1:p.Glu251=
XM_011528133.1:c.461A=	XP_011526435.1:p.Glu154=
XM_017026989.1:c.1031A=	XP_016882478.1:p.Glu344=
XM_017026990.1:c.752A=	XP_016882479.1:p.Glu251=
NM_030662.4:c.1031A= MANE Select	NP_109587.1:p.Glu344=