Canonical Allele Identifier: CA2319222235

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095392T= , CM000681.2:g.4095392T=	GRCh38
NC_000019.9:g.4095390T= , CM000681.1:g.4095390T=	GRCh37
NC_000019.8:g.4046390T=	NCBI36
NG_007996.1:g.33737A= , LRG_750:g.33737A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1481A=
ENST00000688002.1:n.3193A=
ENST00000688751.1:n.178A=
ENST00000689792.1:n.946A=
ENST00000262948.10:c.1042A= MANE Select	ENSP00000262948.4:p.Lys348=
ENST00000262948.9:c.1042A=	ENSP00000262948.3:p.Lys348=
ENST00000394867.8:c.751A=	ENSP00000378336.1:p.Lys251=
ENST00000595715.1:n.857A=
ENST00000597263.5:n.227A=
ENST00000599021.1:c.152A=
ENST00000600584.5:n.1602A=
ENST00000601786.5:n.1343A=
NM_030662.3:c.1042A= , LRG_750t1:c.1042A=	NP_109587.1:p.Lys348=
XM_006722799.2:c.763A=	XP_006722862.1:p.Lys255=
XM_011528133.1:c.472A=	XP_011526435.1:p.Lys158=
XM_017026989.1:c.1042A=	XP_016882478.1:p.Lys348=
XM_017026990.1:c.763A=	XP_016882479.1:p.Lys255=
NM_030662.4:c.1042A= MANE Select	NP_109587.1:p.Lys348=