Canonical Allele Identifier: CA2319222250

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095423C= , CM000681.2:g.4095423C=	GRCh38
NC_000019.9:g.4095421C= , CM000681.1:g.4095421C=	GRCh37
NC_000019.8:g.4046421C=	NCBI36
NG_007996.1:g.33706G= , LRG_750:g.33706G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1450G=
ENST00000688002.1:n.3162G=
ENST00000688751.1:n.147G=
ENST00000689792.1:n.915G=
ENST00000262948.10:c.1011G= MANE Select	ENSP00000262948.4:p.Val337=
ENST00000262948.9:c.1011G=	ENSP00000262948.3:p.Val337=
ENST00000394867.8:c.720G=	ENSP00000378336.1:p.Val240=
ENST00000595715.1:n.826G=
ENST00000597263.5:n.196G=
ENST00000599021.1:c.121G=
ENST00000600584.5:n.1571G=
ENST00000601786.5:n.1312G=
NM_030662.3:c.1011G= , LRG_750t1:c.1011G=	NP_109587.1:p.Val337=
XM_006722799.2:c.732G=	XP_006722862.1:p.Val244=
XM_011528133.1:c.441G=	XP_011526435.1:p.Val147=
XM_017026989.1:c.1011G=	XP_016882478.1:p.Val337=
XM_017026990.1:c.732G=	XP_016882479.1:p.Val244=
NM_030662.4:c.1011G= MANE Select	NP_109587.1:p.Val337=