Canonical Allele Identifier: CA2319219724

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090584G= , CM000681.2:g.4090584G=	GRCh38
NC_000019.9:g.4090582G= , CM000681.1:g.4090582G=	GRCh37
NC_000019.8:g.4041582G=	NCBI36
NG_007996.1:g.38545C= , LRG_750:g.38545C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1656C=
ENST00000688002.1:n.3368C=
ENST00000688751.1:n.353C=
ENST00000689792.1:n.1121C=
ENST00000262948.10:c.*14C= MANE Select	ENSP00000262948.4:n.*14C=
ENST00000262948.9:c.*14C=	ENSP00000262948.3:n.*14C=
ENST00000394867.8:c.*14C=	ENSP00000378336.1:n.*14C=
ENST00000597263.5:n.402C=
ENST00000600584.5:n.2666C=
ENST00000601786.5:n.1518C=
NM_030662.3:c.*14C= , LRG_750t1:c.*14C=	NP_109587.1:n.*14C=
XM_006722799.2:c.*14C=	XP_006722862.1:n.*14C=
XM_011528133.1:c.*14C=	XP_011526435.1:n.*14C=
NM_030662.4:c.*14C= MANE Select	NP_109587.1:n.*14C=