Canonical Allele Identifier: CA2319224453

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099397_4099398delinsGC , CM000681.2:g.4099397_4099398delinsGC	GRCh38
NC_000019.9:g.4099395_4099396delinsGC , CM000681.1:g.4099395_4099396delinsGC	GRCh37
NC_000019.8:g.4050395_4050396delinsGC	NCBI36
NG_007996.1:g.29731_29732delinsGC , LRG_750:g.29731_29732delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1161_1162delinsGC
ENST00000687128.1:n.1161_1162delinsGC
ENST00000688002.1:n.1016_1017delinsGC
ENST00000689792.1:n.646-20_646-19delinsGC
ENST00000262948.10:c.722_723delinsGC MANE Select	ENSP00000262948.4:p.Gly241=
ENST00000262948.9:c.722_723delinsGC	ENSP00000262948.3:p.Gly241=
ENST00000394867.8:c.431_432delinsGC	ENSP00000378336.1:p.Gly144=
ENST00000593364.5:n.669_670delinsGC
ENST00000595715.1:n.537_538delinsGC
ENST00000597263.5:n.169+1621_169+1622delinsGC
ENST00000599021.1:c.29+1621_29+1622delinsGC
ENST00000600584.5:n.1282_1283delinsGC
ENST00000601786.5:n.1023_1024delinsGC
NM_030662.3:c.722_723delinsGC , LRG_750t1:c.722_723delinsGC	NP_109587.1:p.Gly241=
XM_006722799.2:c.705+1621_705+1622delinsGC	XP_006722862.1:n.705+1621_705+1622delinsGC
XM_011528133.1:c.152_153delinsGC	XP_011526435.1:p.Gly51=
XM_017026989.1:c.722_723delinsGC	XP_016882478.1:p.Gly241=
XM_017026990.1:c.705+1621_705+1622delinsGC	XP_016882479.1:n.705+1621_705+1622delinsGC
NM_030662.4:c.722_723delinsGC MANE Select	NP_109587.1:p.Gly241=