Canonical Allele Identifier: CA2319222372

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095645_4095646delinsAG , CM000681.2:g.4095645_4095646delinsAG	GRCh38
NC_000019.9:g.4095643_4095644delinsAG , CM000681.1:g.4095643_4095644delinsAG	GRCh37
NC_000019.8:g.4046643_4046644delinsAG	NCBI36
NG_007996.1:g.33483_33484delinsCT , LRG_750:g.33483_33484delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1424-197_1424-196delinsCT
ENST00000688002.1:n.3136-197_3136-196delinsCT
ENST00000688751.1:n.121-197_121-196delinsCT
ENST00000689792.1:n.889-197_889-196delinsCT
ENST00000262948.10:c.985-197_985-196delinsCT MANE Select	ENSP00000262948.4:n.985-197_985-196delinsCT
ENST00000262948.9:c.985-197_985-196delinsCT	ENSP00000262948.3:n.985-197_985-196delinsCT
ENST00000394867.8:c.694-197_694-196delinsCT	ENSP00000378336.1:n.694-197_694-196delinsCT
ENST00000595715.1:n.800-197_800-196delinsCT
ENST00000597263.5:n.170-197_170-196delinsCT
ENST00000599021.1:c.95-197_95-196delinsCT
ENST00000600584.5:n.1545-197_1545-196delinsCT
ENST00000601786.5:n.1286-197_1286-196delinsCT
NM_030662.3:c.985-197_985-196delinsCT , LRG_750t1:c.985-197_985-196delinsCT	NP_109587.1:n.985-197_985-196delinsCT
XM_006722799.2:c.706-197_706-196delinsCT	XP_006722862.1:n.706-197_706-196delinsCT
XM_011528133.1:c.415-197_415-196delinsCT	XP_011526435.1:n.415-197_415-196delinsCT
XM_017026989.1:c.985-197_985-196delinsCT	XP_016882478.1:n.985-197_985-196delinsCT
XM_017026990.1:c.706-197_706-196delinsCT	XP_016882479.1:n.706-197_706-196delinsCT
NM_030662.4:c.985-197_985-196delinsCT MANE Select	NP_109587.1:n.985-197_985-196delinsCT