Canonical Allele Identifier: CA2319234339

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117562_4117563delinsGC , CM000681.2:g.4117562_4117563delinsGC	GRCh38
NC_000019.9:g.4117560_4117561delinsGC , CM000681.1:g.4117560_4117561delinsGC	GRCh37
NC_000019.8:g.4068560_4068561delinsGC	NCBI36
NG_007996.1:g.11566_11567delinsGC , LRG_750:g.11566_11567delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.598_599delinsGC
ENST00000687128.1:n.598_599delinsGC
ENST00000262948.10:c.159_160delinsGC MANE Select	ENSP00000262948.4:p.Arg53=
ENST00000262948.9:c.159_160delinsGC	ENSP00000262948.3:p.Arg53=
ENST00000394867.8:c.-133_-132delinsGC	ENSP00000378336.1:n.-133_-132delinsGC
ENST00000599345.1:n.356_357delinsGC
NM_030662.3:c.159_160delinsGC , LRG_750t1:c.159_160delinsGC	NP_109587.1:p.Arg53=
XM_006722799.2:c.159_160delinsGC	XP_006722862.1:p.Arg53=
XM_017026989.1:c.159_160delinsGC	XP_016882478.1:p.Arg53=
XM_017026990.1:c.159_160delinsGC	XP_016882479.1:p.Arg53=
XM_017026991.1:c.159_160delinsGC	XP_016882480.1:p.Arg53=
NM_030662.4:c.159_160delinsGC MANE Select	NP_109587.1:p.Arg53=