Canonical Allele Identifier: CA2319221790

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094660G= , CM000681.2:g.4094660G=	GRCh38
NC_000019.9:g.4094658G= , CM000681.1:g.4094658G=	GRCh37
NC_000019.8:g.4045658G=	NCBI36
NG_007996.1:g.34469C= , LRG_750:g.34469C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-162C=
ENST00000688002.1:n.3198-162C=
ENST00000688751.1:n.183-162C=
ENST00000689792.1:n.951-162C=
ENST00000262948.10:c.1047-162C= MANE Select	ENSP00000262948.4:n.1047-162C=
ENST00000262948.9:c.1047-162C=	ENSP00000262948.3:n.1047-162C=
ENST00000394867.8:c.756-162C=	ENSP00000378336.1:n.756-162C=
ENST00000597263.5:n.232-162C=
ENST00000599021.1:c.157-162C=
ENST00000600584.5:n.2334C=
ENST00000601786.5:n.1348-162C=
NM_030662.3:c.1047-162C= , LRG_750t1:c.1047-162C=	NP_109587.1:n.1047-162C=
XM_006722799.2:c.768-162C=	XP_006722862.1:n.768-162C=
XM_011528133.1:c.477-162C=	XP_011526435.1:n.477-162C=
XM_017026989.1:c.1433C=	XP_016882478.1:p.Pro478=
XM_017026990.1:c.1154C=	XP_016882479.1:p.Pro385=
NM_030662.4:c.1047-162C= MANE Select	NP_109587.1:n.1047-162C=