Canonical Allele Identifier: CA2319234363

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117628C= , CM000681.2:g.4117628C=	GRCh38
NC_000019.9:g.4117626C= , CM000681.1:g.4117626C=	GRCh37
NC_000019.8:g.4068626C=	NCBI36
NG_007996.1:g.11501G= , LRG_750:g.11501G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.533G=
ENST00000687128.1:n.533G=
ENST00000262948.10:c.94G= MANE Select	ENSP00000262948.4:p.Ala32=
ENST00000262948.9:c.94G=	ENSP00000262948.3:p.Ala32=
ENST00000394867.8:c.-198G=	ENSP00000378336.1:n.-198G=
ENST00000599345.1:n.291G=
NM_030662.3:c.94G= , LRG_750t1:c.94G=	NP_109587.1:p.Ala32=
XM_006722799.2:c.94G=	XP_006722862.1:p.Ala32=
XM_017026989.1:c.94G=	XP_016882478.1:p.Ala32=
XM_017026990.1:c.94G=	XP_016882479.1:p.Ala32=
XM_017026991.1:c.94G=	XP_016882480.1:p.Ala32=
NM_030662.4:c.94G= MANE Select	NP_109587.1:p.Ala32=