Canonical Allele Identifier: CA2319219761
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090639G= , CM000681.2:g.4090639G= GRCh38
NC_000019.9:g.4090637G= , CM000681.1:g.4090637G= GRCh37
NC_000019.8:g.4041637G= NCBI36
NG_007996.1:g.38490C= , LRG_750:g.38490C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1601C=
ENST00000688002.1:n.3313C=
ENST00000688751.1:n.298C=
ENST00000689792.1:n.1066C=
ENST00000262948.10:c.1162C= MANE Select ENSP00000262948.4:p.Arg388=
ENST00000262948.9:c.1162C= ENSP00000262948.3:p.Arg388=
ENST00000394867.8:c.871C= ENSP00000378336.1:p.Arg291=
ENST00000597263.5:n.347C=
ENST00000599021.1:c.272C=
ENST00000600584.5:n.2611C=
ENST00000601786.5:n.1463C=
NM_030662.3:c.1162C= , LRG_750t1:c.1162C= NP_109587.1:p.Arg388=
XM_006722799.2:c.883C= XP_006722862.1:p.Arg295=
XM_011528133.1:c.592C= XP_011526435.1:p.Arg198=
NM_030662.4:c.1162C= MANE Select NP_109587.1:p.Arg388=