Canonical Allele Identifier: CA2319222113

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095181G= , CM000681.2:g.4095181G=	GRCh38
NC_000019.9:g.4095179G= , CM000681.1:g.4095179G=	GRCh37
NC_000019.8:g.4046179G=	NCBI36
NG_007996.1:g.33948C= , LRG_750:g.33948C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1485+207C=
ENST00000688002.1:n.3197+207C=
ENST00000688751.1:n.182+207C=
ENST00000689792.1:n.950+207C=
ENST00000262948.10:c.1046+207C= MANE Select	ENSP00000262948.4:n.1046+207C=
ENST00000262948.9:c.1046+207C=	ENSP00000262948.3:n.1046+207C=
ENST00000394867.8:c.755+207C=	ENSP00000378336.1:n.755+207C=
ENST00000597263.5:n.231+207C=
ENST00000599021.1:c.156+207C=
ENST00000600584.5:n.1813C=
ENST00000601786.5:n.1347+207C=
NM_030662.3:c.1046+207C= , LRG_750t1:c.1046+207C=	NP_109587.1:n.1046+207C=
XM_006722799.2:c.767+207C=	XP_006722862.1:n.767+207C=
XM_011528133.1:c.476+207C=	XP_011526435.1:n.476+207C=
XM_017026989.1:c.1047-135C=	XP_016882478.1:n.1047-135C=
XM_017026990.1:c.768-135C=	XP_016882479.1:n.768-135C=
NM_030662.4:c.1046+207C= MANE Select	NP_109587.1:n.1046+207C=