Canonical Allele Identifier: CA2319221693
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4094482C= , CM000681.2:g.4094482C= GRCh38
NC_000019.9:g.4094480C= , CM000681.1:g.4094480C= GRCh37
NC_000019.8:g.4045480C= NCBI36
NG_007996.1:g.34647G= , LRG_750:g.34647G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1502G=
ENST00000688002.1:n.3214G=
ENST00000688751.1:n.199G=
ENST00000689792.1:n.967G=
ENST00000262948.10:c.1063G= MANE Select ENSP00000262948.4:p.Ala355=
ENST00000262948.9:c.1063G= ENSP00000262948.3:p.Ala355=
ENST00000394867.8:c.772G= ENSP00000378336.1:p.Ala258=
ENST00000597263.5:n.248G=
ENST00000599021.1:c.173G=
ENST00000600584.5:n.2512G=
ENST00000601786.5:n.1364G=
NM_030662.3:c.1063G= , LRG_750t1:c.1063G= NP_109587.1:p.Ala355=
XM_006722799.2:c.784G= XP_006722862.1:p.Ala262=
XM_011528133.1:c.493G= XP_011526435.1:p.Ala165=
NM_030662.4:c.1063G= MANE Select NP_109587.1:p.Ala355=