Canonical Allele Identifier: CA2319221698

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094494T= , CM000681.2:g.4094494T=	GRCh38
NC_000019.9:g.4094492T= , CM000681.1:g.4094492T=	GRCh37
NC_000019.8:g.4045492T=	NCBI36
NG_007996.1:g.34635A= , LRG_750:g.34635A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1490A=
ENST00000688002.1:n.3202A=
ENST00000688751.1:n.187A=
ENST00000689792.1:n.955A=
ENST00000262948.10:c.1051A= MANE Select	ENSP00000262948.4:p.Ile351=
ENST00000262948.9:c.1051A=	ENSP00000262948.3:p.Ile351=
ENST00000394867.8:c.760A=	ENSP00000378336.1:p.Ile254=
ENST00000597263.5:n.236A=
ENST00000599021.1:c.161A=
ENST00000600584.5:n.2500A=
ENST00000601786.5:n.1352A=
NM_030662.3:c.1051A= , LRG_750t1:c.1051A=	NP_109587.1:p.Ile351=
XM_006722799.2:c.772A=	XP_006722862.1:p.Ile258=
XM_011528133.1:c.481A=	XP_011526435.1:p.Ile161=
NM_030662.4:c.1051A= MANE Select	NP_109587.1:p.Ile351=