Canonical Allele Identifier: CA2319222254

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095428C= , CM000681.2:g.4095428C=	GRCh38
NC_000019.9:g.4095426C= , CM000681.1:g.4095426C=	GRCh37
NC_000019.8:g.4046426C=	NCBI36
NG_007996.1:g.33701G= , LRG_750:g.33701G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1445G=
ENST00000688002.1:n.3157G=
ENST00000688751.1:n.142G=
ENST00000689792.1:n.910G=
ENST00000262948.10:c.1006G= MANE Select	ENSP00000262948.4:p.Gly336=
ENST00000262948.9:c.1006G=	ENSP00000262948.3:p.Gly336=
ENST00000394867.8:c.715G=	ENSP00000378336.1:p.Gly239=
ENST00000595715.1:n.821G=
ENST00000597263.5:n.191G=
ENST00000599021.1:c.116G=
ENST00000600584.5:n.1566G=
ENST00000601786.5:n.1307G=
NM_030662.3:c.1006G= , LRG_750t1:c.1006G=	NP_109587.1:p.Gly336=
XM_006722799.2:c.727G=	XP_006722862.1:p.Gly243=
XM_011528133.1:c.436G=	XP_011526435.1:p.Gly146=
XM_017026989.1:c.1006G=	XP_016882478.1:p.Gly336=
XM_017026990.1:c.727G=	XP_016882479.1:p.Gly243=
NM_030662.4:c.1006G= MANE Select	NP_109587.1:p.Gly336=