Canonical Allele Identifier: CA2319222260

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095445G= , CM000681.2:g.4095445G=	GRCh38
NC_000019.9:g.4095443G= , CM000681.1:g.4095443G=	GRCh37
NC_000019.8:g.4046443G=	NCBI36
NG_007996.1:g.33684C= , LRG_750:g.33684C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1428C=
ENST00000688002.1:n.3140C=
ENST00000688751.1:n.125C=
ENST00000689792.1:n.893C=
ENST00000262948.10:c.989C= MANE Select	ENSP00000262948.4:p.Pro330=
ENST00000262948.9:c.989C=	ENSP00000262948.3:p.Pro330=
ENST00000394867.8:c.698C=	ENSP00000378336.1:p.Pro233=
ENST00000595715.1:n.804C=
ENST00000597263.5:n.174C=
ENST00000599021.1:c.99C=
ENST00000600584.5:n.1549C=
ENST00000601786.5:n.1290C=
NM_030662.3:c.989C= , LRG_750t1:c.989C=	NP_109587.1:p.Pro330=
XM_006722799.2:c.710C=	XP_006722862.1:p.Pro237=
XM_011528133.1:c.419C=	XP_011526435.1:p.Pro140=
XM_017026989.1:c.989C=	XP_016882478.1:p.Pro330=
XM_017026990.1:c.710C=	XP_016882479.1:p.Pro237=
NM_030662.4:c.989C= MANE Select	NP_109587.1:p.Pro330=