Canonical Allele Identifier: CA2319224447

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099381G= , CM000681.2:g.4099381G=	GRCh38
NC_000019.9:g.4099379G= , CM000681.1:g.4099379G=	GRCh37
NC_000019.8:g.4050379G=	NCBI36
NG_007996.1:g.29748C= , LRG_750:g.29748C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1178C=
ENST00000687128.1:n.1178C=
ENST00000688002.1:n.1033C=
ENST00000689792.1:n.646-3C=
ENST00000262948.10:c.739C= MANE Select	ENSP00000262948.4:p.Gln247=
ENST00000262948.9:c.739C=	ENSP00000262948.3:p.Gln247=
ENST00000394867.8:c.448C=	ENSP00000378336.1:p.Gln150=
ENST00000593364.5:n.686C=
ENST00000595715.1:n.554C=
ENST00000597263.5:n.169+1638C=
ENST00000599021.1:c.29+1638C=
ENST00000600584.5:n.1299C=
ENST00000601786.5:n.1040C=
NM_030662.3:c.739C= , LRG_750t1:c.739C=	NP_109587.1:p.Gln247=
XM_006722799.2:c.705+1638C=	XP_006722862.1:n.705+1638C=
XM_011528133.1:c.169C=	XP_011526435.1:p.Gln57=
XM_017026989.1:c.739C=	XP_016882478.1:p.Gln247=
XM_017026990.1:c.705+1638C=	XP_016882479.1:n.705+1638C=
NM_030662.4:c.739C= MANE Select	NP_109587.1:p.Gln247=