Canonical Allele Identifier: CA2319224534

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099551A= , CM000681.2:g.4099551A=	GRCh38
NC_000019.9:g.4099549A= , CM000681.1:g.4099549A=	GRCh37
NC_000019.8:g.4050549A=	NCBI36
NG_007996.1:g.29578T= , LRG_750:g.29578T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-137T=
ENST00000687128.1:n.1145-137T=
ENST00000688002.1:n.863T=
ENST00000689792.1:n.646-173T=
ENST00000262948.10:c.706-137T= MANE Select	ENSP00000262948.4:n.706-137T=
ENST00000262948.9:c.706-137T=	ENSP00000262948.3:n.706-137T=
ENST00000394867.8:c.415-137T=	ENSP00000378336.1:n.415-137T=
ENST00000593364.5:n.653-137T=
ENST00000595715.1:n.384T=
ENST00000597263.5:n.169+1468T=
ENST00000599021.1:c.29+1468T=
ENST00000600584.5:n.1129T=
ENST00000601786.5:n.1007-137T=
ENST00000602167.5:n.426-137T=
NM_030662.3:c.706-137T= , LRG_750t1:c.706-137T=	NP_109587.1:n.706-137T=
XM_006722799.2:c.705+1468T=	XP_006722862.1:n.705+1468T=
XM_011528133.1:c.136-137T=	XP_011526435.1:n.136-137T=
XM_017026989.1:c.706-137T=	XP_016882478.1:n.706-137T=
XM_017026990.1:c.705+1468T=	XP_016882479.1:n.705+1468T=
XM_017026991.1:c.*179T=	XP_016882480.1:n.*179T=
NM_030662.4:c.706-137T= MANE Select	NP_109587.1:n.706-137T=