Canonical Allele Identifier: CA2319225381

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4101032C= , CM000681.2:g.4101032C=	GRCh38
NC_000019.9:g.4101030C= , CM000681.1:g.4101030C=	GRCh37
NC_000019.8:g.4052030C=	NCBI36
NG_007996.1:g.28097G= , LRG_750:g.28097G=

Transcript Alleles

HGVS	Amino-acid Change
NM_030662.4:c.692G= MANE Select	NP_109587.1:p.Arg231=
ENST00000262948.10:c.692G= MANE Select	ENSP00000262948.4:p.Arg231=
NM_030662.3:c.692G= , LRG_750t1:c.692G=	NP_109587.1:p.Arg231=
ENST00000262948.9:c.692G=	ENSP00000262948.3:p.Arg231=
ENST00000394867.8:c.401G=	ENSP00000378336.1:p.Arg134=
ENST00000394867.9:n.1131G=
ENST00000593364.5:n.639G=
ENST00000597008.5:n.293G=
ENST00000597263.5:n.156G=
ENST00000599021.1:c.16G=
ENST00000601786.5:n.993G=
ENST00000602167.5:n.412G=
ENST00000687128.1:n.1131G=
ENST00000689792.1:n.632G=
XM_006722799.2:c.692G=	XP_006722862.1:p.Arg231=
XM_011528133.1:c.122G=	XP_011526435.1:p.Arg41=
XM_017026989.1:c.692G=	XP_016882478.1:p.Arg231=
XM_017026990.1:c.692G=	XP_016882479.1:p.Arg231=
XM_017026991.1:c.692G=	XP_016882480.1:p.Arg231=