Canonical Allele Identifier: CA2319224312

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099156_4099167delinsAGGGCACTGCGC , CM000681.2:g.4099156_4099167delinsAGGGCACTGCGC	GRCh38
NC_000019.9:g.4099154_4099165delinsAGGGCACTGCGC , CM000681.1:g.4099154_4099165delinsAGGGCACTGCGC	GRCh37
NC_000019.8:g.4050154_4050165delinsAGGGCACTGCGC	NCBI36
NG_007996.1:g.29962_29973delinsGCGCAGTGCCCT , LRG_750:g.29962_29973delinsGCGCAGTGCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358+34_1358+45delinsGCGCAGTGCCCT
ENST00000687128.1:n.1392_1403delinsGCGCAGTGCCCT
ENST00000688002.1:n.1247_1258delinsGCGCAGTGCCCT
ENST00000689792.1:n.823+34_823+45delinsGCGCAGTGCCCT
ENST00000262948.10:c.919+34_919+45delinsGCGCAGTGCCCT MANE Select	ENSP00000262948.4:n.919+34_919+45delinsGCGCAGTGCCCT
ENST00000262948.9:c.919+34_919+45delinsGCGCAGTGCCCT	ENSP00000262948.3:n.919+34_919+45delinsGCGCAGTGCCCT
ENST00000394867.8:c.628+34_628+45delinsGCGCAGTGCCCT	ENSP00000378336.1:n.628+34_628+45delinsGCGCAGTGCCCT
ENST00000595715.1:n.734+34_734+45delinsGCGCAGTGCCCT
ENST00000597263.5:n.169+1852_169+1863delinsGCGCAGTGCCCT
ENST00000599021.1:c.30-1824_30-1813delinsGCGCAGTGCCCT
ENST00000600584.5:n.1479+34_1479+45delinsGCGCAGTGCCCT
ENST00000601786.5:n.1220+34_1220+45delinsGCGCAGTGCCCT
NM_030662.3:c.919+34_919+45delinsGCGCAGTGCCCT , LRG_750t1:c.919+34_919+45delinsGCGCAGTGCCCT	NP_109587.1:n.919+34_919+45delinsGCGCAGTGCCCT
XM_006722799.2:c.705+1852_705+1863delinsGCGCAGTGCCCT	XP_006722862.1:n.705+1852_705+1863delinsGCGCAGTGCCCT
XM_011528133.1:c.349+34_349+45delinsGCGCAGTGCCCT	XP_011526435.1:n.349+34_349+45delinsGCGCAGTGCCCT
XM_017026989.1:c.919+34_919+45delinsGCGCAGTGCCCT	XP_016882478.1:n.919+34_919+45delinsGCGCAGTGCCCT
XM_017026990.1:c.705+1852_705+1863delinsGCGCAGTGCCCT	XP_016882479.1:n.705+1852_705+1863delinsGCGCAGTGCCCT
NM_030662.4:c.919+34_919+45delinsGCGCAGTGCCCT MANE Select	NP_109587.1:n.919+34_919+45delinsGCGCAGTGCCCT