Canonical Allele Identifier: CA2319224465

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099427_4099429delinsCAG , CM000681.2:g.4099427_4099429delinsCAG	GRCh38
NC_000019.9:g.4099425_4099427delinsCAG , CM000681.1:g.4099425_4099427delinsCAG	GRCh37
NC_000019.8:g.4050425_4050427delinsCAG	NCBI36
NG_007996.1:g.29700_29702delinsCTG , LRG_750:g.29700_29702delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-15_1145-13delinsCTG
ENST00000687128.1:n.1145-15_1145-13delinsCTG
ENST00000688002.1:n.985_987delinsCTG
ENST00000689792.1:n.646-51_646-49delinsCTG
ENST00000262948.10:c.706-15_706-13delinsCTG MANE Select	ENSP00000262948.4:n.706-15_706-13delinsCTG
ENST00000262948.9:c.706-15_706-13delinsCTG	ENSP00000262948.3:n.706-15_706-13delinsCTG
ENST00000394867.8:c.415-15_415-13delinsCTG	ENSP00000378336.1:n.415-15_415-13delinsCTG
ENST00000593364.5:n.653-15_653-13delinsCTG
ENST00000595715.1:n.506_508delinsCTG
ENST00000597263.5:n.169+1590_169+1592delinsCTG
ENST00000599021.1:c.29+1590_29+1592delinsCTG
ENST00000600584.5:n.1251_1253delinsCTG
ENST00000601786.5:n.1007-15_1007-13delinsCTG
ENST00000602167.5:n.426-15_426-13delinsCTG
NM_030662.3:c.706-15_706-13delinsCTG , LRG_750t1:c.706-15_706-13delinsCTG	NP_109587.1:n.706-15_706-13delinsCTG
XM_006722799.2:c.705+1590_705+1592delinsCTG	XP_006722862.1:n.705+1590_705+1592delinsCTG
XM_011528133.1:c.136-15_136-13delinsCTG	XP_011526435.1:n.136-15_136-13delinsCTG
XM_017026989.1:c.706-15_706-13delinsCTG	XP_016882478.1:n.706-15_706-13delinsCTG
XM_017026990.1:c.705+1590_705+1592delinsCTG	XP_016882479.1:n.705+1590_705+1592delinsCTG
NM_030662.4:c.706-15_706-13delinsCTG MANE Select	NP_109587.1:n.706-15_706-13delinsCTG