Canonical Allele Identifier: CA2319222367

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095642_4095648delinsTAGAGGG , CM000681.2:g.4095642_4095648delinsTAGAGGG	GRCh38
NC_000019.9:g.4095640_4095646delinsTAGAGGG , CM000681.1:g.4095640_4095646delinsTAGAGGG	GRCh37
NC_000019.8:g.4046640_4046646delinsTAGAGGG	NCBI36
NG_007996.1:g.33481_33487delinsCCCTCTA , LRG_750:g.33481_33487delinsCCCTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1424-199_1424-193delinsCCCTCTA
ENST00000688002.1:n.3136-199_3136-193delinsCCCTCTA
ENST00000688751.1:n.121-199_121-193delinsCCCTCTA
ENST00000689792.1:n.889-199_889-193delinsCCCTCTA
ENST00000262948.10:c.985-199_985-193delinsCCCTCTA MANE Select	ENSP00000262948.4:n.985-199_985-193delinsCCCTCTA
ENST00000262948.9:c.985-199_985-193delinsCCCTCTA	ENSP00000262948.3:n.985-199_985-193delinsCCCTCTA
ENST00000394867.8:c.694-199_694-193delinsCCCTCTA	ENSP00000378336.1:n.694-199_694-193delinsCCCTCTA
ENST00000595715.1:n.800-199_800-193delinsCCCTCTA
ENST00000597263.5:n.170-199_170-193delinsCCCTCTA
ENST00000599021.1:c.95-199_95-193delinsCCCTCTA
ENST00000600584.5:n.1545-199_1545-193delinsCCCTCTA
ENST00000601786.5:n.1286-199_1286-193delinsCCCTCTA
NM_030662.3:c.985-199_985-193delinsCCCTCTA , LRG_750t1:c.985-199_985-193delinsCCCTCTA	NP_109587.1:n.985-199_985-193delinsCCCTCTA
XM_006722799.2:c.706-199_706-193delinsCCCTCTA	XP_006722862.1:n.706-199_706-193delinsCCCTCTA
XM_011528133.1:c.415-199_415-193delinsCCCTCTA	XP_011526435.1:n.415-199_415-193delinsCCCTCTA
XM_017026989.1:c.985-199_985-193delinsCCCTCTA	XP_016882478.1:n.985-199_985-193delinsCCCTCTA
XM_017026990.1:c.706-199_706-193delinsCCCTCTA	XP_016882479.1:n.706-199_706-193delinsCCCTCTA
NM_030662.4:c.985-199_985-193delinsCCCTCTA MANE Select	NP_109587.1:n.985-199_985-193delinsCCCTCTA