Canonical Allele Identifier: CA2319221539

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094199G= , CM000681.2:g.4094199G=	GRCh38
NC_000019.9:g.4094197G= , CM000681.1:g.4094197G=	GRCh37
NC_000019.8:g.4045197G=	NCBI36
NG_007996.1:g.34930C= , LRG_750:g.34930C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1531+254C=
ENST00000688002.1:n.3243+254C=
ENST00000688751.1:n.228+254C=
ENST00000689792.1:n.996+254C=
ENST00000262948.10:c.1092+254C= MANE Select	ENSP00000262948.4:n.1092+254C=
ENST00000262948.9:c.1092+254C=	ENSP00000262948.3:n.1092+254C=
ENST00000394867.8:c.801+254C=	ENSP00000378336.1:n.801+254C=
ENST00000597263.5:n.277+254C=
ENST00000599021.1:c.202+254C=
ENST00000600584.5:n.2541+254C=
ENST00000601786.5:n.1393+254C=
NM_030662.3:c.1092+254C= , LRG_750t1:c.1092+254C=	NP_109587.1:n.1092+254C=
XM_006722799.2:c.813+254C=	XP_006722862.1:n.813+254C=
XM_011528133.1:c.522+254C=	XP_011526435.1:n.522+254C=
NM_030662.4:c.1092+254C= MANE Select	NP_109587.1:n.1092+254C=