Canonical Allele Identifier: CA2319219736

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090606C= , CM000681.2:g.4090606C=	GRCh38
NC_000019.9:g.4090604C= , CM000681.1:g.4090604C=	GRCh37
NC_000019.8:g.4041604C=	NCBI36
NG_007996.1:g.38523G= , LRG_750:g.38523G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1634G=
ENST00000688002.1:n.3346G=
ENST00000688751.1:n.331G=
ENST00000689792.1:n.1099G=
ENST00000262948.10:c.1195G= MANE Select	ENSP00000262948.4:p.Ala399=
ENST00000262948.9:c.1195G=	ENSP00000262948.3:p.Ala399=
ENST00000394867.8:c.904G=	ENSP00000378336.1:p.Ala302=
ENST00000597263.5:n.380G=
ENST00000599021.1:c.305G=
ENST00000600584.5:n.2644G=
ENST00000601786.5:n.1496G=
NM_030662.3:c.1195G= , LRG_750t1:c.1195G=	NP_109587.1:p.Ala399=
XM_006722799.2:c.916G=	XP_006722862.1:p.Ala306=
XM_011528133.1:c.625G=	XP_011526435.1:p.Ala209=
NM_030662.4:c.1195G= MANE Select	NP_109587.1:p.Ala399=