Canonical Allele Identifier: CA2584878557

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4099471-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099474del , CM000681.2:g.4099474del	GRCh38
NC_000019.9:g.4099472del , CM000681.1:g.4099472del	GRCh37
NC_000019.8:g.4050472del	NCBI36
NG_007996.1:g.29657del , LRG_750:g.29657del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-58del
ENST00000687128.1:n.1145-58del
ENST00000688002.1:n.942del
ENST00000689792.1:n.646-94del
ENST00000262948.10:c.706-58del MANE Select	ENSP00000262948.4:n.706-58del
ENST00000262948.9:c.706-58del	ENSP00000262948.3:n.706-58del
ENST00000394867.8:c.415-58del	ENSP00000378336.1:n.415-58del
ENST00000593364.5:n.653-58del
ENST00000595715.1:n.463del
ENST00000597263.5:n.169+1547del
ENST00000599021.1:c.29+1547del
ENST00000600584.5:n.1208del
ENST00000601786.5:n.1007-58del
ENST00000602167.5:n.426-58del
NM_030662.3:c.706-58del , LRG_750t1:c.706-58del	NP_109587.1:n.706-58del
XM_006722799.2:c.705+1547del	XP_006722862.1:n.705+1547del
XM_011528133.1:c.136-58del	XP_011526435.1:n.136-58del
XM_017026989.1:c.706-58del	XP_016882478.1:n.706-58del
XM_017026990.1:c.705+1547del	XP_016882479.1:n.705+1547del
XM_017026991.1:c.*258del	XP_016882480.1:n.*258del
NM_030662.4:c.706-58del MANE Select	NP_109587.1:n.706-58del