Canonical Allele Identifier: CA2319221697
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4094493A= , CM000681.2:g.4094493A= GRCh38
NC_000019.9:g.4094491A= , CM000681.1:g.4094491A= GRCh37
NC_000019.8:g.4045491A= NCBI36
NG_007996.1:g.34636T= , LRG_750:g.34636T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1491T=
ENST00000688002.1:n.3203T=
ENST00000688751.1:n.188T=
ENST00000689792.1:n.956T=
ENST00000262948.10:c.1052T= MANE Select ENSP00000262948.4:p.Ile351=
ENST00000262948.9:c.1052T= ENSP00000262948.3:p.Ile351=
ENST00000394867.8:c.761T= ENSP00000378336.1:p.Ile254=
ENST00000597263.5:n.237T=
ENST00000599021.1:c.162T=
ENST00000600584.5:n.2501T=
ENST00000601786.5:n.1353T=
NM_030662.3:c.1052T= , LRG_750t1:c.1052T= NP_109587.1:p.Ile351=
XM_006722799.2:c.773T= XP_006722862.1:p.Ile258=
XM_011528133.1:c.482T= XP_011526435.1:p.Ile161=
NM_030662.4:c.1052T= MANE Select NP_109587.1:p.Ile351=