Canonical Allele Identifier: CA2319219662

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090481C= , CM000681.2:g.4090481C=	GRCh38
NC_000019.9:g.4090479C= , CM000681.1:g.4090479C=	GRCh37
NC_000019.8:g.4041479C=	NCBI36
NG_007996.1:g.38648G= , LRG_750:g.38648G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1759G=
ENST00000688002.1:n.3471G=
ENST00000688751.1:n.456G=
ENST00000689792.1:n.1224G=
ENST00000262948.10:c.*117G= MANE Select	ENSP00000262948.4:n.*117G=
ENST00000262948.9:c.*117G=	ENSP00000262948.3:n.*117G=
ENST00000394867.8:c.*117G=	ENSP00000378336.1:n.*117G=
ENST00000597263.5:n.505G=
ENST00000600584.5:n.2769G=
ENST00000601786.5:n.1621G=
NM_030662.3:c.*117G= , LRG_750t1:c.*117G=	NP_109587.1:n.*117G=
XM_006722799.2:c.*117G=	XP_006722862.1:n.*117G=
XM_011528133.1:c.*117G=	XP_011526435.1:n.*117G=
NM_030662.4:c.*117G= MANE Select	NP_109587.1:n.*117G=