Canonical Allele Identifier: CA2319230728

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4110467C= , CM000681.2:g.4110467C=	GRCh38
NC_000019.9:g.4110465C= , CM000681.1:g.4110465C=	GRCh37
NC_000019.8:g.4061465C=	NCBI36
NG_007996.1:g.18662G= , LRG_750:g.18662G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.889+42G=
ENST00000687128.1:n.889+42G=
ENST00000262948.10:c.450+42G= MANE Select	ENSP00000262948.4:n.450+42G=
ENST00000262948.9:c.450+42G=	ENSP00000262948.3:n.450+42G=
ENST00000394867.8:c.159+42G=	ENSP00000378336.1:n.159+42G=
ENST00000599345.1:n.647+42G=
NM_030662.3:c.450+42G= , LRG_750t1:c.450+42G=	NP_109587.1:n.450+42G=
XM_006722799.2:c.450+42G=	XP_006722862.1:n.450+42G=
XM_017026989.1:c.450+42G=	XP_016882478.1:n.450+42G=
XM_017026990.1:c.450+42G=	XP_016882479.1:n.450+42G=
XM_017026991.1:c.450+42G=	XP_016882480.1:n.450+42G=
NM_030662.4:c.450+42G= MANE Select	NP_109587.1:n.450+42G=