Canonical Allele Identifier: CA2319230218

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4110572G= , CM000681.2:g.4110572G=	GRCh38
NC_000019.9:g.4110570G= , CM000681.1:g.4110570G=	GRCh37
NC_000019.8:g.4061570G=	NCBI36
NG_007996.1:g.18557C= , LRG_750:g.18557C=

Transcript Alleles

HGVS	Amino-acid Change
NM_030662.4:c.387C= MANE Select	NP_109587.1:p.Tyr129=
ENST00000262948.10:c.387C= MANE Select	ENSP00000262948.4:p.Tyr129=
NM_030662.3:c.387C= , LRG_750t1:c.387C=	NP_109587.1:p.Tyr129=
ENST00000262948.9:c.387C=	ENSP00000262948.3:p.Tyr129=
ENST00000394867.8:c.96C=	ENSP00000378336.1:p.Tyr32=
ENST00000394867.9:n.826C=
ENST00000599345.1:n.584C=
ENST00000687128.1:n.826C=
XM_006722799.2:c.387C=	XP_006722862.1:p.Tyr129=
XM_017026989.1:c.387C=	XP_016882478.1:p.Tyr129=
XM_017026990.1:c.387C=	XP_016882479.1:p.Tyr129=
XM_017026991.1:c.387C=	XP_016882480.1:p.Tyr129=