Canonical Allele Identifier: CA2319219733

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090603C= , CM000681.2:g.4090603C=	GRCh38
NC_000019.9:g.4090601C= , CM000681.1:g.4090601C=	GRCh37
NC_000019.8:g.4041601C=	NCBI36
NG_007996.1:g.38526G= , LRG_750:g.38526G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1637G=
ENST00000688002.1:n.3349G=
ENST00000688751.1:n.334G=
ENST00000689792.1:n.1102G=
ENST00000262948.10:c.1198G= MANE Select	ENSP00000262948.4:p.Val400=
ENST00000262948.9:c.1198G=	ENSP00000262948.3:p.Val400=
ENST00000394867.8:c.907G=	ENSP00000378336.1:p.Val303=
ENST00000597263.5:n.383G=
ENST00000599021.1:c.308G=
ENST00000600584.5:n.2647G=
ENST00000601786.5:n.1499G=
NM_030662.3:c.1198G= , LRG_750t1:c.1198G=	NP_109587.1:p.Val400=
XM_006722799.2:c.919G=	XP_006722862.1:p.Val307=
XM_011528133.1:c.628G=	XP_011526435.1:p.Val210=
NM_030662.4:c.1198G= MANE Select	NP_109587.1:p.Val400=