Canonical Allele Identifier: CA2319221573

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094259_4094260delinsGC , CM000681.2:g.4094259_4094260delinsGC	GRCh38
NC_000019.9:g.4094257_4094258delinsGC , CM000681.1:g.4094257_4094258delinsGC	GRCh37
NC_000019.8:g.4045257_4045258delinsGC	NCBI36
NG_007996.1:g.34869_34870delinsGC , LRG_750:g.34869_34870delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1531+193_1531+194delinsGC
ENST00000688002.1:n.3243+193_3243+194delinsGC
ENST00000688751.1:n.228+193_228+194delinsGC
ENST00000689792.1:n.996+193_996+194delinsGC
ENST00000262948.10:c.1092+193_1092+194delinsGC MANE Select	ENSP00000262948.4:n.1092+193_1092+194delinsGC
ENST00000262948.9:c.1092+193_1092+194delinsGC	ENSP00000262948.3:n.1092+193_1092+194delinsGC
ENST00000394867.8:c.801+193_801+194delinsGC	ENSP00000378336.1:n.801+193_801+194delinsGC
ENST00000597263.5:n.277+193_277+194delinsGC
ENST00000599021.1:c.202+193_202+194delinsGC
ENST00000600584.5:n.2541+193_2541+194delinsGC
ENST00000601786.5:n.1393+193_1393+194delinsGC
NM_030662.3:c.1092+193_1092+194delinsGC , LRG_750t1:c.1092+193_1092+194delinsGC	NP_109587.1:n.1092+193_1092+194delinsGC
XM_006722799.2:c.813+193_813+194delinsGC	XP_006722862.1:n.813+193_813+194delinsGC
XM_011528133.1:c.522+193_522+194delinsGC	XP_011526435.1:n.522+193_522+194delinsGC
NM_030662.4:c.1092+193_1092+194delinsGC MANE Select	NP_109587.1:n.1092+193_1092+194delinsGC