Canonical Allele Identifier: CA2319224515

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099521C= , CM000681.2:g.4099521C=	GRCh38
NC_000019.9:g.4099519C= , CM000681.1:g.4099519C=	GRCh37
NC_000019.8:g.4050519C=	NCBI36
NG_007996.1:g.29608G= , LRG_750:g.29608G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-107G=
ENST00000687128.1:n.1145-107G=
ENST00000688002.1:n.893G=
ENST00000689792.1:n.646-143G=
ENST00000262948.10:c.706-107G= MANE Select	ENSP00000262948.4:n.706-107G=
ENST00000262948.9:c.706-107G=	ENSP00000262948.3:n.706-107G=
ENST00000394867.8:c.415-107G=	ENSP00000378336.1:n.415-107G=
ENST00000593364.5:n.653-107G=
ENST00000595715.1:n.414G=
ENST00000597263.5:n.169+1498G=
ENST00000599021.1:c.29+1498G=
ENST00000600584.5:n.1159G=
ENST00000601786.5:n.1007-107G=
ENST00000602167.5:n.426-107G=
NM_030662.3:c.706-107G= , LRG_750t1:c.706-107G=	NP_109587.1:n.706-107G=
XM_006722799.2:c.705+1498G=	XP_006722862.1:n.705+1498G=
XM_011528133.1:c.136-107G=	XP_011526435.1:n.136-107G=
XM_017026989.1:c.706-107G=	XP_016882478.1:n.706-107G=
XM_017026990.1:c.705+1498G=	XP_016882479.1:n.705+1498G=
XM_017026991.1:c.*209G=	XP_016882480.1:n.*209G=
NM_030662.4:c.706-107G= MANE Select	NP_109587.1:n.706-107G=