Canonical Allele Identifier: CA2584877082

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4094625-G-GATCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094626_4094627insTCCA , CM000681.2:g.4094626_4094627insTCCA	GRCh38
NC_000019.9:g.4094624_4094625insTCCA , CM000681.1:g.4094624_4094625insTCCA	GRCh37
NC_000019.8:g.4045624_4045625insTCCA	NCBI36
NG_007996.1:g.34503_34504insGGAT , LRG_750:g.34503_34504insGGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-128_1486-127insGGAT
ENST00000688002.1:n.3198-128_3198-127insGGAT
ENST00000688751.1:n.183-128_183-127insGGAT
ENST00000689792.1:n.951-128_951-127insGGAT
ENST00000262948.10:c.1047-128_1047-127insGGAT MANE Select	ENSP00000262948.4:n.1047-128_1047-127insGGAT
ENST00000262948.9:c.1047-128_1047-127insGGAT	ENSP00000262948.3:n.1047-128_1047-127insGGAT
ENST00000394867.8:c.756-128_756-127insGGAT	ENSP00000378336.1:n.756-128_756-127insGGAT
ENST00000597263.5:n.232-128_232-127insGGAT
ENST00000599021.1:c.157-128_157-127insGGAT
ENST00000600584.5:n.2368_2369insGGAT
ENST00000601786.5:n.1348-128_1348-127insGGAT
NM_030662.3:c.1047-128_1047-127insGGAT , LRG_750t1:c.1047-128_1047-127insGGAT	NP_109587.1:n.1047-128_1047-127insGGAT
XM_006722799.2:c.768-128_768-127insGGAT	XP_006722862.1:n.768-128_768-127insGGAT
XM_011528133.1:c.477-128_477-127insGGAT	XP_011526435.1:n.477-128_477-127insGGAT
XM_017026989.1:c.1467_1468insGGAT	XP_016882478.1:p.Leu490GlyfsTer?
XM_017026990.1:c.1188_1189insGGAT	XP_016882479.1:p.Leu397GlyfsTer?
NM_030662.4:c.1047-128_1047-127insGGAT MANE Select	NP_109587.1:n.1047-128_1047-127insGGAT