Canonical Allele Identifier: CA2319219772
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090658G= , CM000681.2:g.4090658G= GRCh38
NC_000019.9:g.4090656G= , CM000681.1:g.4090656G= GRCh37
NC_000019.8:g.4041656G= NCBI36
NG_007996.1:g.38471C= , LRG_750:g.38471C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1582C=
ENST00000688002.1:n.3294C=
ENST00000688751.1:n.279C=
ENST00000689792.1:n.1047C=
ENST00000262948.10:c.1143C= MANE Select ENSP00000262948.4:p.Gly381=
ENST00000262948.9:c.1143C= ENSP00000262948.3:p.Gly381=
ENST00000394867.8:c.852C= ENSP00000378336.1:p.Gly284=
ENST00000597263.5:n.328C=
ENST00000599021.1:c.253C=
ENST00000600584.5:n.2592C=
ENST00000601786.5:n.1444C=
NM_030662.3:c.1143C= , LRG_750t1:c.1143C= NP_109587.1:p.Gly381=
XM_006722799.2:c.864C= XP_006722862.1:p.Gly288=
XM_011528133.1:c.573C= XP_011526435.1:p.Gly191=
NM_030662.4:c.1143C= MANE Select NP_109587.1:p.Gly381=