Canonical Allele Identifier: CA2319224358

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099214C= , CM000681.2:g.4099214C=	GRCh38
NC_000019.9:g.4099212C= , CM000681.1:g.4099212C=	GRCh37
NC_000019.8:g.4050212C=	NCBI36
NG_007996.1:g.29915G= , LRG_750:g.29915G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1345G=
ENST00000687128.1:n.1345G=
ENST00000688002.1:n.1200G=
ENST00000689792.1:n.810G=
ENST00000262948.10:c.906G= MANE Select	ENSP00000262948.4:p.Gly302=
ENST00000262948.9:c.906G=	ENSP00000262948.3:p.Gly302=
ENST00000394867.8:c.615G=	ENSP00000378336.1:p.Gly205=
ENST00000593364.5:n.853G=
ENST00000595715.1:n.721G=
ENST00000597263.5:n.169+1805G=
ENST00000599021.1:c.29+1805G=
ENST00000600584.5:n.1466G=
ENST00000601786.5:n.1207G=
NM_030662.3:c.906G= , LRG_750t1:c.906G=	NP_109587.1:p.Gly302=
XM_006722799.2:c.705+1805G=	XP_006722862.1:n.705+1805G=
XM_011528133.1:c.336G=	XP_011526435.1:p.Gly112=
XM_017026989.1:c.906G=	XP_016882478.1:p.Gly302=
XM_017026990.1:c.705+1805G=	XP_016882479.1:n.705+1805G=
NM_030662.4:c.906G= MANE Select	NP_109587.1:p.Gly302=