Canonical Allele Identifier: CA2319219786

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090689C= , CM000681.2:g.4090689C=	GRCh38
NC_000019.9:g.4090687C= , CM000681.1:g.4090687C=	GRCh37
NC_000019.8:g.4041687C=	NCBI36
NG_007996.1:g.38440G= , LRG_750:g.38440G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1551G=
ENST00000688002.1:n.3263G=
ENST00000688751.1:n.248G=
ENST00000689792.1:n.1016G=
ENST00000262948.10:c.1112G= MANE Select	ENSP00000262948.4:p.Arg371=
ENST00000262948.9:c.1112G=	ENSP00000262948.3:p.Arg371=
ENST00000394867.8:c.821G=	ENSP00000378336.1:p.Arg274=
ENST00000597263.5:n.297G=
ENST00000599021.1:c.222G=
ENST00000600584.5:n.2561G=
ENST00000601786.5:n.1413G=
NM_030662.3:c.1112G= , LRG_750t1:c.1112G=	NP_109587.1:p.Arg371=
XM_006722799.2:c.833G=	XP_006722862.1:p.Arg278=
XM_011528133.1:c.542G=	XP_011526435.1:p.Arg181=
NM_030662.4:c.1112G= MANE Select	NP_109587.1:p.Arg371=