Canonical Allele Identifier: CA2319219762
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090641A= , CM000681.2:g.4090641A= GRCh38
NC_000019.9:g.4090639A= , CM000681.1:g.4090639A= GRCh37
NC_000019.8:g.4041639A= NCBI36
NG_007996.1:g.38488T= , LRG_750:g.38488T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1599T=
ENST00000688002.1:n.3311T=
ENST00000688751.1:n.296T=
ENST00000689792.1:n.1064T=
ENST00000262948.10:c.1160T= MANE Select ENSP00000262948.4:p.Leu387=
ENST00000262948.9:c.1160T= ENSP00000262948.3:p.Leu387=
ENST00000394867.8:c.869T= ENSP00000378336.1:p.Leu290=
ENST00000597263.5:n.345T=
ENST00000599021.1:c.270T=
ENST00000600584.5:n.2609T=
ENST00000601786.5:n.1461T=
NM_030662.3:c.1160T= , LRG_750t1:c.1160T= NP_109587.1:p.Leu387=
XM_006722799.2:c.881T= XP_006722862.1:p.Leu294=
XM_011528133.1:c.590T= XP_011526435.1:p.Leu197=
NM_030662.4:c.1160T= MANE Select NP_109587.1:p.Leu387=