Canonical Allele Identifier: CA2319219753

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090624C= , CM000681.2:g.4090624C=	GRCh38
NC_000019.9:g.4090622C= , CM000681.1:g.4090622C=	GRCh37
NC_000019.8:g.4041622C=	NCBI36
NG_007996.1:g.38505G= , LRG_750:g.38505G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1616G=
ENST00000688002.1:n.3328G=
ENST00000688751.1:n.313G=
ENST00000689792.1:n.1081G=
ENST00000262948.10:c.1177G= MANE Select	ENSP00000262948.4:p.Gly393=
ENST00000262948.9:c.1177G=	ENSP00000262948.3:p.Gly393=
ENST00000394867.8:c.886G=	ENSP00000378336.1:p.Gly296=
ENST00000597263.5:n.362G=
ENST00000599021.1:c.287G=
ENST00000600584.5:n.2626G=
ENST00000601786.5:n.1478G=
NM_030662.3:c.1177G= , LRG_750t1:c.1177G=	NP_109587.1:p.Gly393=
XM_006722799.2:c.898G=	XP_006722862.1:p.Gly300=
XM_011528133.1:c.607G=	XP_011526435.1:p.Gly203=
NM_030662.4:c.1177G= MANE Select	NP_109587.1:p.Gly393=