Canonical Allele Identifier: CA2319224411

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099302T= , CM000681.2:g.4099302T=	GRCh38
NC_000019.9:g.4099300T= , CM000681.1:g.4099300T=	GRCh37
NC_000019.8:g.4050300T=	NCBI36
NG_007996.1:g.29827A= , LRG_750:g.29827A=

Transcript Alleles

HGVS	Amino-acid Change
NM_030662.4:c.818A= MANE Select	NP_109587.1:p.Lys273=
ENST00000262948.10:c.818A= MANE Select	ENSP00000262948.4:p.Lys273=
NM_030662.3:c.818A= , LRG_750t1:c.818A=	NP_109587.1:p.Lys273=
ENST00000262948.9:c.818A=	ENSP00000262948.3:p.Lys273=
ENST00000394867.8:c.527A=	ENSP00000378336.1:p.Lys176=
ENST00000394867.9:n.1257A=
ENST00000593364.5:n.765A=
ENST00000595715.1:n.633A=
ENST00000597263.5:n.169+1717A=
ENST00000599021.1:c.29+1717A=
ENST00000600584.5:n.1378A=
ENST00000601786.5:n.1119A=
ENST00000687128.1:n.1257A=
ENST00000688002.1:n.1112A=
ENST00000689792.1:n.722A=
XM_006722799.2:c.705+1717A=	XP_006722862.1:n.705+1717A=
XM_011528133.1:c.248A=	XP_011526435.1:p.Lys83=
XM_017026989.1:c.818A=	XP_016882478.1:p.Lys273=
XM_017026990.1:c.705+1717A=	XP_016882479.1:n.705+1717A=