Canonical Allele Identifier: CA2319224452

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099397G= , CM000681.2:g.4099397G=	GRCh38
NC_000019.9:g.4099395G= , CM000681.1:g.4099395G=	GRCh37
NC_000019.8:g.4050395G=	NCBI36
NG_007996.1:g.29732C= , LRG_750:g.29732C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1162C=
ENST00000687128.1:n.1162C=
ENST00000688002.1:n.1017C=
ENST00000689792.1:n.646-19C=
ENST00000262948.10:c.723C= MANE Select	ENSP00000262948.4:p.Gly241=
ENST00000262948.9:c.723C=	ENSP00000262948.3:p.Gly241=
ENST00000394867.8:c.432C=	ENSP00000378336.1:p.Gly144=
ENST00000593364.5:n.670C=
ENST00000595715.1:n.538C=
ENST00000597263.5:n.169+1622C=
ENST00000599021.1:c.29+1622C=
ENST00000600584.5:n.1283C=
ENST00000601786.5:n.1024C=
NM_030662.3:c.723C= , LRG_750t1:c.723C=	NP_109587.1:p.Gly241=
XM_006722799.2:c.705+1622C=	XP_006722862.1:n.705+1622C=
XM_011528133.1:c.153C=	XP_011526435.1:p.Gly51=
XM_017026989.1:c.723C=	XP_016882478.1:p.Gly241=
XM_017026990.1:c.705+1622C=	XP_016882479.1:n.705+1622C=
NM_030662.4:c.723C= MANE Select	NP_109587.1:p.Gly241=