Canonical Allele Identifier: CA2319221767

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094615C= , CM000681.2:g.4094615C=	GRCh38
NC_000019.9:g.4094613C= , CM000681.1:g.4094613C=	GRCh37
NC_000019.8:g.4045613C=	NCBI36
NG_007996.1:g.34514G= , LRG_750:g.34514G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-117G=
ENST00000688002.1:n.3198-117G=
ENST00000688751.1:n.183-117G=
ENST00000689792.1:n.951-117G=
ENST00000262948.10:c.1047-117G= MANE Select	ENSP00000262948.4:n.1047-117G=
ENST00000262948.9:c.1047-117G=	ENSP00000262948.3:n.1047-117G=
ENST00000394867.8:c.756-117G=	ENSP00000378336.1:n.756-117G=
ENST00000597263.5:n.232-117G=
ENST00000599021.1:c.157-117G=
ENST00000600584.5:n.2379G=
ENST00000601786.5:n.1348-117G=
NM_030662.3:c.1047-117G= , LRG_750t1:c.1047-117G=	NP_109587.1:n.1047-117G=
XM_006722799.2:c.768-117G=	XP_006722862.1:n.768-117G=
XM_011528133.1:c.477-117G=	XP_011526435.1:n.477-117G=
XM_017026989.1:c.1478G=	XP_016882478.1:p.Arg493=
XM_017026990.1:c.1199G=	XP_016882479.1:p.Arg400=
NM_030662.4:c.1047-117G= MANE Select	NP_109587.1:n.1047-117G=