Canonical Allele Identifier: CA2319224451

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099395G= , CM000681.2:g.4099395G=	GRCh38
NC_000019.9:g.4099393G= , CM000681.1:g.4099393G=	GRCh37
NC_000019.8:g.4050393G=	NCBI36
NG_007996.1:g.29734C= , LRG_750:g.29734C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1164C=
ENST00000687128.1:n.1164C=
ENST00000688002.1:n.1019C=
ENST00000689792.1:n.646-17C=
ENST00000262948.10:c.725C= MANE Select	ENSP00000262948.4:p.Thr242=
ENST00000262948.9:c.725C=	ENSP00000262948.3:p.Thr242=
ENST00000394867.8:c.434C=	ENSP00000378336.1:p.Thr145=
ENST00000593364.5:n.672C=
ENST00000595715.1:n.540C=
ENST00000597263.5:n.169+1624C=
ENST00000599021.1:c.29+1624C=
ENST00000600584.5:n.1285C=
ENST00000601786.5:n.1026C=
NM_030662.3:c.725C= , LRG_750t1:c.725C=	NP_109587.1:p.Thr242=
XM_006722799.2:c.705+1624C=	XP_006722862.1:n.705+1624C=
XM_011528133.1:c.155C=	XP_011526435.1:p.Thr52=
XM_017026989.1:c.725C=	XP_016882478.1:p.Thr242=
XM_017026990.1:c.705+1624C=	XP_016882479.1:n.705+1624C=
NM_030662.4:c.725C= MANE Select	NP_109587.1:p.Thr242=