Canonical Allele Identifier: CA2319224232

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4098988_4098989delinsGC , CM000681.2:g.4098988_4098989delinsGC	GRCh38
NC_000019.9:g.4098986_4098987delinsGC , CM000681.1:g.4098986_4098987delinsGC	GRCh37
NC_000019.8:g.4049986_4049987delinsGC	NCBI36
NG_007996.1:g.30140_30141delinsGC , LRG_750:g.30140_30141delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358+212_1358+213delinsGC
ENST00000687128.1:n.1570_1571delinsGC
ENST00000688002.1:n.1425_1426delinsGC
ENST00000689792.1:n.823+212_823+213delinsGC
ENST00000262948.10:c.919+212_919+213delinsGC MANE Select	ENSP00000262948.4:n.919+212_919+213delinsGC
ENST00000262948.9:c.919+212_919+213delinsGC	ENSP00000262948.3:n.919+212_919+213delinsGC
ENST00000394867.8:c.628+212_628+213delinsGC	ENSP00000378336.1:n.628+212_628+213delinsGC
ENST00000595715.1:n.734+212_734+213delinsGC
ENST00000597263.5:n.169+2030_169+2031delinsGC
ENST00000599021.1:c.30-1646_30-1645delinsGC
ENST00000600584.5:n.1479+212_1479+213delinsGC
ENST00000601786.5:n.1220+212_1220+213delinsGC
NM_030662.3:c.919+212_919+213delinsGC , LRG_750t1:c.919+212_919+213delinsGC	NP_109587.1:n.919+212_919+213delinsGC
XM_006722799.2:c.705+2030_705+2031delinsGC	XP_006722862.1:n.705+2030_705+2031delinsGC
XM_011528133.1:c.349+212_349+213delinsGC	XP_011526435.1:n.349+212_349+213delinsGC
XM_017026989.1:c.919+212_919+213delinsGC	XP_016882478.1:n.919+212_919+213delinsGC
XM_017026990.1:c.705+2030_705+2031delinsGC	XP_016882479.1:n.705+2030_705+2031delinsGC
NM_030662.4:c.919+212_919+213delinsGC MANE Select	NP_109587.1:n.919+212_919+213delinsGC