Canonical Allele Identifier: CA2319234359

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117622G= , CM000681.2:g.4117622G=	GRCh38
NC_000019.9:g.4117620G= , CM000681.1:g.4117620G=	GRCh37
NC_000019.8:g.4068620G=	NCBI36
NG_007996.1:g.11507C= , LRG_750:g.11507C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.539C=
ENST00000687128.1:n.539C=
ENST00000262948.10:c.100C= MANE Select	ENSP00000262948.4:p.Leu34=
ENST00000262948.9:c.100C=	ENSP00000262948.3:p.Leu34=
ENST00000394867.8:c.-192C=	ENSP00000378336.1:n.-192C=
ENST00000599345.1:n.297C=
NM_030662.3:c.100C= , LRG_750t1:c.100C=	NP_109587.1:p.Leu34=
XM_006722799.2:c.100C=	XP_006722862.1:p.Leu34=
XM_017026989.1:c.100C=	XP_016882478.1:p.Leu34=
XM_017026990.1:c.100C=	XP_016882479.1:p.Leu34=
XM_017026991.1:c.100C=	XP_016882480.1:p.Leu34=
NM_030662.4:c.100C= MANE Select	NP_109587.1:p.Leu34=