Canonical Allele Identifier: CA2319224375

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099243T= , CM000681.2:g.4099243T=	GRCh38
NC_000019.9:g.4099241T= , CM000681.1:g.4099241T=	GRCh37
NC_000019.8:g.4050241T=	NCBI36
NG_007996.1:g.29886A= , LRG_750:g.29886A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1316A=
ENST00000687128.1:n.1316A=
ENST00000688002.1:n.1171A=
ENST00000689792.1:n.781A=
ENST00000262948.10:c.877A= MANE Select	ENSP00000262948.4:p.Ser293=
ENST00000262948.9:c.877A=	ENSP00000262948.3:p.Ser293=
ENST00000394867.8:c.586A=	ENSP00000378336.1:p.Ser196=
ENST00000593364.5:n.824A=
ENST00000595715.1:n.692A=
ENST00000597263.5:n.169+1776A=
ENST00000599021.1:c.29+1776A=
ENST00000600584.5:n.1437A=
ENST00000601786.5:n.1178A=
NM_030662.3:c.877A= , LRG_750t1:c.877A=	NP_109587.1:p.Ser293=
XM_006722799.2:c.705+1776A=	XP_006722862.1:n.705+1776A=
XM_011528133.1:c.307A=	XP_011526435.1:p.Ser103=
XM_017026989.1:c.877A=	XP_016882478.1:p.Ser293=
XM_017026990.1:c.705+1776A=	XP_016882479.1:n.705+1776A=
NM_030662.4:c.877A= MANE Select	NP_109587.1:p.Ser293=