Canonical Allele Identifier: CA2319224339

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099189_4099191delinsTTC , CM000681.2:g.4099189_4099191delinsTTC	GRCh38
NC_000019.9:g.4099187_4099189delinsTTC , CM000681.1:g.4099187_4099189delinsTTC	GRCh37
NC_000019.8:g.4050187_4050189delinsTTC	NCBI36
NG_007996.1:g.29938_29940delinsGAA , LRG_750:g.29938_29940delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358+10_1358+12delinsGAA
ENST00000687128.1:n.1368_1370delinsGAA
ENST00000688002.1:n.1223_1225delinsGAA
ENST00000689792.1:n.823+10_823+12delinsGAA
ENST00000262948.10:c.919+10_919+12delinsGAA MANE Select	ENSP00000262948.4:n.919+10_919+12delinsGAA
ENST00000262948.9:c.919+10_919+12delinsGAA	ENSP00000262948.3:n.919+10_919+12delinsGAA
ENST00000394867.8:c.628+10_628+12delinsGAA	ENSP00000378336.1:n.628+10_628+12delinsGAA
ENST00000595715.1:n.734+10_734+12delinsGAA
ENST00000597263.5:n.169+1828_169+1830delinsGAA
ENST00000599021.1:c.29+1828_29+1830delinsGAA
ENST00000600584.5:n.1479+10_1479+12delinsGAA
ENST00000601786.5:n.1220+10_1220+12delinsGAA
NM_030662.3:c.919+10_919+12delinsGAA , LRG_750t1:c.919+10_919+12delinsGAA	NP_109587.1:n.919+10_919+12delinsGAA
XM_006722799.2:c.705+1828_705+1830delinsGAA	XP_006722862.1:n.705+1828_705+1830delinsGAA
XM_011528133.1:c.349+10_349+12delinsGAA	XP_011526435.1:n.349+10_349+12delinsGAA
XM_017026989.1:c.919+10_919+12delinsGAA	XP_016882478.1:n.919+10_919+12delinsGAA
XM_017026990.1:c.705+1828_705+1830delinsGAA	XP_016882479.1:n.705+1828_705+1830delinsGAA
NM_030662.4:c.919+10_919+12delinsGAA MANE Select	NP_109587.1:n.919+10_919+12delinsGAA