Canonical Allele Identifier: CA2576573256

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099437del , CM000681.2:g.4099437del	GRCh38
NC_000019.9:g.4099435del , CM000681.1:g.4099435del	GRCh37
NC_000019.8:g.4050435del	NCBI36
NG_007996.1:g.29694del , LRG_750:g.29694del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-21del
ENST00000687128.1:n.1145-21del
ENST00000688002.1:n.979del
ENST00000689792.1:n.646-57del
ENST00000262948.10:c.706-21del MANE Select	ENSP00000262948.4:n.706-21del
ENST00000262948.9:c.706-21del	ENSP00000262948.3:n.706-21del
ENST00000394867.8:c.415-21del	ENSP00000378336.1:n.415-21del
ENST00000593364.5:n.653-21del
ENST00000595715.1:n.500del
ENST00000597263.5:n.169+1584del
ENST00000599021.1:c.29+1584del
ENST00000600584.5:n.1245del
ENST00000601786.5:n.1007-21del
ENST00000602167.5:n.426-21del
NM_030662.3:c.706-21del , LRG_750t1:c.706-21del	NP_109587.1:n.706-21del
XM_006722799.2:c.705+1584del	XP_006722862.1:n.705+1584del
XM_011528133.1:c.136-21del	XP_011526435.1:n.136-21del
XM_017026989.1:c.706-21del	XP_016882478.1:n.706-21del
XM_017026990.1:c.705+1584del	XP_016882479.1:n.705+1584del
XM_017026991.1:c.*295del	XP_016882480.1:n.*295del
NM_030662.4:c.706-21del MANE Select	NP_109587.1:n.706-21del