Canonical Allele Identifier: CA2319221681

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094457A= , CM000681.2:g.4094457A=	GRCh38
NC_000019.9:g.4094455A= , CM000681.1:g.4094455A=	GRCh37
NC_000019.8:g.4045455A=	NCBI36
NG_007996.1:g.34672T= , LRG_750:g.34672T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1527T=
ENST00000688002.1:n.3239T=
ENST00000688751.1:n.224T=
ENST00000689792.1:n.992T=
ENST00000262948.10:c.1088T= MANE Select	ENSP00000262948.4:p.Leu363=
ENST00000262948.9:c.1088T=	ENSP00000262948.3:p.Leu363=
ENST00000394867.8:c.797T=	ENSP00000378336.1:p.Leu266=
ENST00000597263.5:n.273T=
ENST00000599021.1:c.198T=
ENST00000600584.5:n.2537T=
ENST00000601786.5:n.1389T=
NM_030662.3:c.1088T= , LRG_750t1:c.1088T=	NP_109587.1:p.Leu363=
XM_006722799.2:c.809T=	XP_006722862.1:p.Leu270=
XM_011528133.1:c.518T=	XP_011526435.1:p.Leu173=
NM_030662.4:c.1088T= MANE Select	NP_109587.1:p.Leu363=