Canonical Allele Identifier: CA2319224359
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4099216C= , CM000681.2:g.4099216C= GRCh38
NC_000019.9:g.4099214C= , CM000681.1:g.4099214C= GRCh37
NC_000019.8:g.4050214C= NCBI36
NG_007996.1:g.29913G= , LRG_750:g.29913G=

Transcript Alleles

HGVS Amino-acid change
ENST00000394867.9:n.1343G=
ENST00000687128.1:n.1343G=
ENST00000688002.1:n.1198G=
ENST00000689792.1:n.808G=
ENST00000262948.10:c.904G= MANE Select ENSP00000262948.4:p.Gly302=
ENST00000262948.9:c.904G= ENSP00000262948.3:p.Gly302=
ENST00000394867.8:c.613G= ENSP00000378336.1:p.Gly205=
ENST00000593364.5:n.851G=
ENST00000595715.1:n.719G=
ENST00000597263.5:n.169+1803G=
ENST00000599021.1:c.29+1803G=
ENST00000600584.5:n.1464G=
ENST00000601786.5:n.1205G=
NM_030662.3:c.904G= , LRG_750t1:c.904G= NP_109587.1:p.Gly302=
XM_006722799.2:c.705+1803G= XP_006722862.1:n.705+1803G=
XM_011528133.1:c.334G= XP_011526435.1:p.Gly112=
XM_017026989.1:c.904G= XP_016882478.1:p.Gly302=
XM_017026990.1:c.705+1803G= XP_016882479.1:n.705+1803G=
NM_030662.4:c.904G= MANE Select NP_109587.1:p.Gly302=