Canonical Allele Identifier: CA2584878511

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4099218-G-GGGGGCCTCGC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099227_4099228insCGGGGCCTCG , CM000681.2:g.4099227_4099228insCGGGGCCTCG	GRCh38
NC_000019.9:g.4099225_4099226insCGGGGCCTCG , CM000681.1:g.4099225_4099226insCGGGGCCTCG	GRCh37
NC_000019.8:g.4050225_4050226insCGGGGCCTCG	NCBI36
NG_007996.1:g.29910_29911insGCGAGGCCCC , LRG_750:g.29910_29911insGCGAGGCCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1340_1341insGCGAGGCCCC
ENST00000687128.1:n.1340_1341insGCGAGGCCCC
ENST00000688002.1:n.1195_1196insGCGAGGCCCC
ENST00000689792.1:n.805_806insGCGAGGCCCC
ENST00000262948.10:c.901_902insGCGAGGCCCC MANE Select	ENSP00000262948.4:p.Pro301ArgfsTer15
ENST00000262948.9:c.901_902insGCGAGGCCCC	ENSP00000262948.3:p.Pro301ArgfsTer15
ENST00000394867.8:c.610_611insGCGAGGCCCC	ENSP00000378336.1:p.Pro204ArgfsTer15
ENST00000593364.5:n.848_849insGCGAGGCCCC
ENST00000595715.1:n.716_717insGCGAGGCCCC
ENST00000597263.5:n.169+1800_169+1801insGCGAGGCCCC
ENST00000599021.1:c.29+1800_29+1801insGCGAGGCCCC
ENST00000600584.5:n.1461_1462insGCGAGGCCCC
ENST00000601786.5:n.1202_1203insGCGAGGCCCC
NM_030662.3:c.901_902insGCGAGGCCCC , LRG_750t1:c.901_902insGCGAGGCCCC	NP_109587.1:p.Pro301ArgfsTer15
XM_006722799.2:c.705+1800_705+1801insGCGAGGCCCC	XP_006722862.1:n.705+1800_705+1801insGCGAGGCCCC
XM_011528133.1:c.331_332insGCGAGGCCCC	XP_011526435.1:p.Pro111ArgfsTer15
XM_017026989.1:c.901_902insGCGAGGCCCC	XP_016882478.1:p.Pro301ArgfsTer15
XM_017026990.1:c.705+1800_705+1801insGCGAGGCCCC	XP_016882479.1:n.705+1800_705+1801insGCGAGGCCCC
NM_030662.4:c.901_902insGCGAGGCCCC MANE Select	NP_109587.1:p.Pro301ArgfsTer15