Canonical Allele Identifier: CA2319219765
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090650C= , CM000681.2:g.4090650C= GRCh38
NC_000019.9:g.4090648C= , CM000681.1:g.4090648C= GRCh37
NC_000019.8:g.4041648C= NCBI36
NG_007996.1:g.38479G= , LRG_750:g.38479G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1590G=
ENST00000688002.1:n.3302G=
ENST00000688751.1:n.287G=
ENST00000689792.1:n.1055G=
ENST00000262948.10:c.1151G= MANE Select ENSP00000262948.4:p.Cys384=
ENST00000262948.9:c.1151G= ENSP00000262948.3:p.Cys384=
ENST00000394867.8:c.860G= ENSP00000378336.1:p.Cys287=
ENST00000597263.5:n.336G=
ENST00000599021.1:c.261G=
ENST00000600584.5:n.2600G=
ENST00000601786.5:n.1452G=
NM_030662.3:c.1151G= , LRG_750t1:c.1151G= NP_109587.1:p.Cys384=
XM_006722799.2:c.872G= XP_006722862.1:p.Cys291=
XM_011528133.1:c.581G= XP_011526435.1:p.Cys194=
NM_030662.4:c.1151G= MANE Select NP_109587.1:p.Cys384=