Canonical Allele Identifier: CA2319221787

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094637G= , CM000681.2:g.4094637G=	GRCh38
NC_000019.9:g.4094635G= , CM000681.1:g.4094635G=	GRCh37
NC_000019.8:g.4045635G=	NCBI36
NG_007996.1:g.34492C= , LRG_750:g.34492C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-139C=
ENST00000688002.1:n.3198-139C=
ENST00000688751.1:n.183-139C=
ENST00000689792.1:n.951-139C=
ENST00000262948.10:c.1047-139C= MANE Select	ENSP00000262948.4:n.1047-139C=
ENST00000262948.9:c.1047-139C=	ENSP00000262948.3:n.1047-139C=
ENST00000394867.8:c.756-139C=	ENSP00000378336.1:n.756-139C=
ENST00000597263.5:n.232-139C=
ENST00000599021.1:c.157-139C=
ENST00000600584.5:n.2357C=
ENST00000601786.5:n.1348-139C=
NM_030662.3:c.1047-139C= , LRG_750t1:c.1047-139C=	NP_109587.1:n.1047-139C=
XM_006722799.2:c.768-139C=	XP_006722862.1:n.768-139C=
XM_011528133.1:c.477-139C=	XP_011526435.1:n.477-139C=
XM_017026989.1:c.1456C=	XP_016882478.1:p.Leu486=
XM_017026990.1:c.1177C=	XP_016882479.1:p.Leu393=
NM_030662.4:c.1047-139C= MANE Select	NP_109587.1:n.1047-139C=