Canonical Allele Identifier: CA2319224519

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099528A= , CM000681.2:g.4099528A=	GRCh38
NC_000019.9:g.4099526A= , CM000681.1:g.4099526A=	GRCh37
NC_000019.8:g.4050526A=	NCBI36
NG_007996.1:g.29601T= , LRG_750:g.29601T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-114T=
ENST00000687128.1:n.1145-114T=
ENST00000688002.1:n.886T=
ENST00000689792.1:n.646-150T=
ENST00000262948.10:c.706-114T= MANE Select	ENSP00000262948.4:n.706-114T=
ENST00000262948.9:c.706-114T=	ENSP00000262948.3:n.706-114T=
ENST00000394867.8:c.415-114T=	ENSP00000378336.1:n.415-114T=
ENST00000593364.5:n.653-114T=
ENST00000595715.1:n.407T=
ENST00000597263.5:n.169+1491T=
ENST00000599021.1:c.29+1491T=
ENST00000600584.5:n.1152T=
ENST00000601786.5:n.1007-114T=
ENST00000602167.5:n.426-114T=
NM_030662.3:c.706-114T= , LRG_750t1:c.706-114T=	NP_109587.1:n.706-114T=
XM_006722799.2:c.705+1491T=	XP_006722862.1:n.705+1491T=
XM_011528133.1:c.136-114T=	XP_011526435.1:n.136-114T=
XM_017026989.1:c.706-114T=	XP_016882478.1:n.706-114T=
XM_017026990.1:c.705+1491T=	XP_016882479.1:n.705+1491T=
XM_017026991.1:c.*202T=	XP_016882480.1:n.*202T=
NM_030662.4:c.706-114T= MANE Select	NP_109587.1:n.706-114T=