Canonical Allele Identifier: CA658795217

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117564_4117593del , CM000681.2:g.4117564_4117593del	GRCh38
NC_000019.9:g.4117562_4117591del , CM000681.1:g.4117562_4117591del	GRCh37
NC_000019.8:g.4068562_4068591del	NCBI36
NG_007996.1:g.11543_11572del , LRG_750:g.11543_11572del

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.575_604del
ENST00000687128.1:n.575_604del
ENST00000262948.10:c.136_165del MANE Select	ENSP00000262948.4:p.Leu46_Glu55del
ENST00000262948.9:c.136_165del	ENSP00000262948.3:p.Leu46_Glu55del
ENST00000394867.8:c.-156_-127del	ENSP00000378336.1:n.-156_-127del
ENST00000599345.1:n.333_362del
NM_030662.3:c.136_165del , LRG_750t1:c.136_165del	NP_109587.1:p.Leu46_Glu55del
XM_006722799.2:c.136_165del	XP_006722862.1:p.Leu46_Glu55del
XM_017026989.1:c.136_165del	XP_016882478.1:p.Leu46_Glu55del
XM_017026990.1:c.136_165del	XP_016882479.1:p.Leu46_Glu55del
XM_017026991.1:c.136_165del	XP_016882480.1:p.Leu46_Glu55del
NM_030662.4:c.136_165del MANE Select	NP_109587.1:p.Leu46_Glu55del