Canonical Allele Identifier: CA2319224422

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099325G= , CM000681.2:g.4099325G=	GRCh38
NC_000019.9:g.4099323G= , CM000681.1:g.4099323G=	GRCh37
NC_000019.8:g.4050323G=	NCBI36
NG_007996.1:g.29804C= , LRG_750:g.29804C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1234C=
ENST00000687128.1:n.1234C=
ENST00000688002.1:n.1089C=
ENST00000689792.1:n.699C=
ENST00000262948.10:c.795C= MANE Select	ENSP00000262948.4:p.Tyr265=
ENST00000262948.9:c.795C=	ENSP00000262948.3:p.Tyr265=
ENST00000394867.8:c.504C=	ENSP00000378336.1:p.Tyr168=
ENST00000593364.5:n.742C=
ENST00000595715.1:n.610C=
ENST00000597263.5:n.169+1694C=
ENST00000599021.1:c.29+1694C=
ENST00000600584.5:n.1355C=
ENST00000601786.5:n.1096C=
NM_030662.3:c.795C= , LRG_750t1:c.795C=	NP_109587.1:p.Tyr265=
XM_006722799.2:c.705+1694C=	XP_006722862.1:n.705+1694C=
XM_011528133.1:c.225C=	XP_011526435.1:p.Tyr75=
XM_017026989.1:c.795C=	XP_016882478.1:p.Tyr265=
XM_017026990.1:c.705+1694C=	XP_016882479.1:n.705+1694C=
NM_030662.4:c.795C= MANE Select	NP_109587.1:p.Tyr265=