Canonical Allele Identifier: CA2319224455

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099407C= , CM000681.2:g.4099407C=	GRCh38
NC_000019.9:g.4099405C= , CM000681.1:g.4099405C=	GRCh37
NC_000019.8:g.4050405C=	NCBI36
NG_007996.1:g.29722G= , LRG_750:g.29722G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1152G=
ENST00000687128.1:n.1152G=
ENST00000688002.1:n.1007G=
ENST00000689792.1:n.646-29G=
ENST00000262948.10:c.713G= MANE Select	ENSP00000262948.4:p.Arg238=
ENST00000262948.9:c.713G=	ENSP00000262948.3:p.Arg238=
ENST00000394867.8:c.422G=	ENSP00000378336.1:p.Arg141=
ENST00000593364.5:n.660G=
ENST00000595715.1:n.528G=
ENST00000597263.5:n.169+1612G=
ENST00000599021.1:c.29+1612G=
ENST00000600584.5:n.1273G=
ENST00000601786.5:n.1014G=
NM_030662.3:c.713G= , LRG_750t1:c.713G=	NP_109587.1:p.Arg238=
XM_006722799.2:c.705+1612G=	XP_006722862.1:n.705+1612G=
XM_011528133.1:c.143G=	XP_011526435.1:p.Arg48=
XM_017026989.1:c.713G=	XP_016882478.1:p.Arg238=
XM_017026990.1:c.705+1612G=	XP_016882479.1:n.705+1612G=
NM_030662.4:c.713G= MANE Select	NP_109587.1:p.Arg238=