Canonical Allele Identifier: CA2319230686

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4110396_4110400delinsAAGCC , CM000681.2:g.4110396_4110400delinsAAGCC	GRCh38
NC_000019.9:g.4110394_4110398delinsAAGCC , CM000681.1:g.4110394_4110398delinsAAGCC	GRCh37
NC_000019.8:g.4061394_4061398delinsAAGCC	NCBI36
NG_007996.1:g.18729_18733delinsGGCTT , LRG_750:g.18729_18733delinsGGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.889+109_889+113delinsGGCTT
ENST00000687128.1:n.889+109_889+113delinsGGCTT
ENST00000262948.10:c.450+109_450+113delinsGGCTT MANE Select	ENSP00000262948.4:n.450+109_450+113delinsGGCTT
ENST00000262948.9:c.450+109_450+113delinsGGCTT	ENSP00000262948.3:n.450+109_450+113delinsGGCTT
ENST00000394867.8:c.159+109_159+113delinsGGCTT	ENSP00000378336.1:n.159+109_159+113delinsGGCTT
ENST00000599345.1:n.647+109_647+113delinsGGCTT
NM_030662.3:c.450+109_450+113delinsGGCTT , LRG_750t1:c.450+109_450+113delinsGGCTT	NP_109587.1:n.450+109_450+113delinsGGCTT
XM_006722799.2:c.450+109_450+113delinsGGCTT	XP_006722862.1:n.450+109_450+113delinsGGCTT
XM_017026989.1:c.450+109_450+113delinsGGCTT	XP_016882478.1:n.450+109_450+113delinsGGCTT
XM_017026990.1:c.450+109_450+113delinsGGCTT	XP_016882479.1:n.450+109_450+113delinsGGCTT
XM_017026991.1:c.450+109_450+113delinsGGCTT	XP_016882480.1:n.450+109_450+113delinsGGCTT
NM_030662.4:c.450+109_450+113delinsGGCTT MANE Select	NP_109587.1:n.450+109_450+113delinsGGCTT