Canonical Allele Identifier: CA2319224492

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099477G= , CM000681.2:g.4099477G=	GRCh38
NC_000019.9:g.4099475G= , CM000681.1:g.4099475G=	GRCh37
NC_000019.8:g.4050475G=	NCBI36
NG_007996.1:g.29652C= , LRG_750:g.29652C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-63C=
ENST00000687128.1:n.1145-63C=
ENST00000688002.1:n.937C=
ENST00000689792.1:n.646-99C=
ENST00000262948.10:c.706-63C= MANE Select	ENSP00000262948.4:n.706-63C=
ENST00000262948.9:c.706-63C=	ENSP00000262948.3:n.706-63C=
ENST00000394867.8:c.415-63C=	ENSP00000378336.1:n.415-63C=
ENST00000593364.5:n.653-63C=
ENST00000595715.1:n.458C=
ENST00000597263.5:n.169+1542C=
ENST00000599021.1:c.29+1542C=
ENST00000600584.5:n.1203C=
ENST00000601786.5:n.1007-63C=
ENST00000602167.5:n.426-63C=
NM_030662.3:c.706-63C= , LRG_750t1:c.706-63C=	NP_109587.1:n.706-63C=
XM_006722799.2:c.705+1542C=	XP_006722862.1:n.705+1542C=
XM_011528133.1:c.136-63C=	XP_011526435.1:n.136-63C=
XM_017026989.1:c.706-63C=	XP_016882478.1:n.706-63C=
XM_017026990.1:c.705+1542C=	XP_016882479.1:n.705+1542C=
XM_017026991.1:c.*253C=	XP_016882480.1:n.*253C=
NM_030662.4:c.706-63C= MANE Select	NP_109587.1:n.706-63C=