Canonical Allele Identifier: CA2584877007

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4094568-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094568_4094569insA , CM000681.2:g.4094568_4094569insA	GRCh38
NC_000019.9:g.4094566_4094567insA , CM000681.1:g.4094566_4094567insA	GRCh37
NC_000019.8:g.4045566_4045567insA	NCBI36
NG_007996.1:g.34560_34561insT , LRG_750:g.34560_34561insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-71_1486-70insT
ENST00000688002.1:n.3198-71_3198-70insT
ENST00000688751.1:n.183-71_183-70insT
ENST00000689792.1:n.951-71_951-70insT
ENST00000262948.10:c.1047-71_1047-70insT MANE Select	ENSP00000262948.4:n.1047-71_1047-70insT
ENST00000262948.9:c.1047-71_1047-70insT	ENSP00000262948.3:n.1047-71_1047-70insT
ENST00000394867.8:c.756-71_756-70insT	ENSP00000378336.1:n.756-71_756-70insT
ENST00000597263.5:n.232-71_232-70insT
ENST00000599021.1:c.157-71_157-70insT
ENST00000600584.5:n.2425_2426insT
ENST00000601786.5:n.1348-71_1348-70insT
NM_030662.3:c.1047-71_1047-70insT , LRG_750t1:c.1047-71_1047-70insT	NP_109587.1:n.1047-71_1047-70insT
XM_006722799.2:c.768-71_768-70insT	XP_006722862.1:n.768-71_768-70insT
XM_011528133.1:c.477-71_477-70insT	XP_011526435.1:n.477-71_477-70insT
XM_017026989.1:c.1524_1525insT	XP_016882478.1:p.Gly509TrpfsTer?
XM_017026990.1:c.1245_1246insT	XP_016882479.1:p.Gly416TrpfsTer?
NM_030662.4:c.1047-71_1047-70insT MANE Select	NP_109587.1:n.1047-71_1047-70insT