Canonical Allele Identifier: CA2319224521

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099534_4099536delinsTAG , CM000681.2:g.4099534_4099536delinsTAG	GRCh38
NC_000019.9:g.4099532_4099534delinsTAG , CM000681.1:g.4099532_4099534delinsTAG	GRCh37
NC_000019.8:g.4050532_4050534delinsTAG	NCBI36
NG_007996.1:g.29593_29595delinsCTA , LRG_750:g.29593_29595delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1145-122_1145-120delinsCTA
ENST00000687128.1:n.1145-122_1145-120delinsCTA
ENST00000688002.1:n.878_880delinsCTA
ENST00000689792.1:n.646-158_646-156delinsCTA
ENST00000262948.10:c.706-122_706-120delinsCTA MANE Select	ENSP00000262948.4:n.706-122_706-120delinsCTA
ENST00000262948.9:c.706-122_706-120delinsCTA	ENSP00000262948.3:n.706-122_706-120delinsCTA
ENST00000394867.8:c.415-122_415-120delinsCTA	ENSP00000378336.1:n.415-122_415-120delinsCTA
ENST00000593364.5:n.653-122_653-120delinsCTA
ENST00000595715.1:n.399_401delinsCTA
ENST00000597263.5:n.169+1483_169+1485delinsCTA
ENST00000599021.1:c.29+1483_29+1485delinsCTA
ENST00000600584.5:n.1144_1146delinsCTA
ENST00000601786.5:n.1007-122_1007-120delinsCTA
ENST00000602167.5:n.426-122_426-120delinsCTA
NM_030662.3:c.706-122_706-120delinsCTA , LRG_750t1:c.706-122_706-120delinsCTA	NP_109587.1:n.706-122_706-120delinsCTA
XM_006722799.2:c.705+1483_705+1485delinsCTA	XP_006722862.1:n.705+1483_705+1485delinsCTA
XM_011528133.1:c.136-122_136-120delinsCTA	XP_011526435.1:n.136-122_136-120delinsCTA
XM_017026989.1:c.706-122_706-120delinsCTA	XP_016882478.1:n.706-122_706-120delinsCTA
XM_017026990.1:c.705+1483_705+1485delinsCTA	XP_016882479.1:n.705+1483_705+1485delinsCTA
XM_017026991.1:c.*194_*196delinsCTA	XP_016882480.1:n.*194_*196delinsCTA
NM_030662.4:c.706-122_706-120delinsCTA MANE Select	NP_109587.1:n.706-122_706-120delinsCTA