Canonical Allele Identifier: CA2319224387

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099263C= , CM000681.2:g.4099263C=	GRCh38
NC_000019.9:g.4099261C= , CM000681.1:g.4099261C=	GRCh37
NC_000019.8:g.4050261C=	NCBI36
NG_007996.1:g.29866G= , LRG_750:g.29866G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1296G=
ENST00000687128.1:n.1296G=
ENST00000688002.1:n.1151G=
ENST00000689792.1:n.761G=
ENST00000262948.10:c.857G= MANE Select	ENSP00000262948.4:p.Gly286=
ENST00000262948.9:c.857G=	ENSP00000262948.3:p.Gly286=
ENST00000394867.8:c.566G=	ENSP00000378336.1:p.Gly189=
ENST00000593364.5:n.804G=
ENST00000595715.1:n.672G=
ENST00000597263.5:n.169+1756G=
ENST00000599021.1:c.29+1756G=
ENST00000600584.5:n.1417G=
ENST00000601786.5:n.1158G=
NM_030662.3:c.857G= , LRG_750t1:c.857G=	NP_109587.1:p.Gly286=
XM_006722799.2:c.705+1756G=	XP_006722862.1:n.705+1756G=
XM_011528133.1:c.287G=	XP_011526435.1:p.Gly96=
XM_017026989.1:c.857G=	XP_016882478.1:p.Gly286=
XM_017026990.1:c.705+1756G=	XP_016882479.1:n.705+1756G=
NM_030662.4:c.857G= MANE Select	NP_109587.1:p.Gly286=