Canonical Allele Identifier: CA2319219683

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090519C= , CM000681.2:g.4090519C=	GRCh38
NC_000019.9:g.4090517C= , CM000681.1:g.4090517C=	GRCh37
NC_000019.8:g.4041517C=	NCBI36
NG_007996.1:g.38610G= , LRG_750:g.38610G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1721G=
ENST00000688002.1:n.3433G=
ENST00000688751.1:n.418G=
ENST00000689792.1:n.1186G=
ENST00000262948.10:c.*79G= MANE Select	ENSP00000262948.4:n.*79G=
ENST00000262948.9:c.*79G=	ENSP00000262948.3:n.*79G=
ENST00000394867.8:c.*79G=	ENSP00000378336.1:n.*79G=
ENST00000597263.5:n.467G=
ENST00000600584.5:n.2731G=
ENST00000601786.5:n.1583G=
NM_030662.3:c.*79G= , LRG_750t1:c.*79G=	NP_109587.1:n.*79G=
XM_006722799.2:c.*79G=	XP_006722862.1:n.*79G=
XM_011528133.1:c.*79G=	XP_011526435.1:n.*79G=
NM_030662.4:c.*79G= MANE Select	NP_109587.1:n.*79G=