Canonical Allele Identifier: CA2319224348

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099201C= , CM000681.2:g.4099201C=	GRCh38
NC_000019.9:g.4099199C= , CM000681.1:g.4099199C=	GRCh37
NC_000019.8:g.4050199C=	NCBI36
NG_007996.1:g.29928G= , LRG_750:g.29928G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358G=
ENST00000687128.1:n.1358G=
ENST00000688002.1:n.1213G=
ENST00000689792.1:n.823G=
ENST00000262948.10:c.919G= MANE Select	ENSP00000262948.4:p.Gly307=
ENST00000262948.9:c.919G=	ENSP00000262948.3:p.Gly307=
ENST00000394867.8:c.628G=	ENSP00000378336.1:p.Gly210=
ENST00000593364.5:n.866G=
ENST00000595715.1:n.734G=
ENST00000597263.5:n.169+1818G=
ENST00000599021.1:c.29+1818G=
ENST00000600584.5:n.1479G=
ENST00000601786.5:n.1220G=
NM_030662.3:c.919G= , LRG_750t1:c.919G=	NP_109587.1:p.Gly307=
XM_006722799.2:c.705+1818G=	XP_006722862.1:n.705+1818G=
XM_011528133.1:c.349G=	XP_011526435.1:p.Gly117=
XM_017026989.1:c.919G=	XP_016882478.1:p.Gly307=
XM_017026990.1:c.705+1818G=	XP_016882479.1:n.705+1818G=
NM_030662.4:c.919G= MANE Select	NP_109587.1:p.Gly307=