Canonical Allele Identifier: CA2813355847

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095517_4095518del , CM000681.2:g.4095517_4095518del	GRCh38
NC_000019.9:g.4095515_4095516del , CM000681.1:g.4095515_4095516del	GRCh37
NC_000019.8:g.4046515_4046516del	NCBI36
NG_007996.1:g.33615_33616del , LRG_750:g.33615_33616del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1424-65_1424-64del
ENST00000688002.1:n.3136-65_3136-64del
ENST00000688751.1:n.121-65_121-64del
ENST00000689792.1:n.889-65_889-64del
ENST00000262948.10:c.985-65_985-64del MANE Select	ENSP00000262948.4:n.985-65_985-64del
ENST00000262948.9:c.985-65_985-64del	ENSP00000262948.3:n.985-65_985-64del
ENST00000394867.8:c.694-65_694-64del	ENSP00000378336.1:n.694-65_694-64del
ENST00000595715.1:n.800-65_800-64del
ENST00000597263.5:n.170-65_170-64del
ENST00000599021.1:c.95-65_95-64del
ENST00000600584.5:n.1545-65_1545-64del
ENST00000601786.5:n.1286-65_1286-64del
NM_030662.3:c.985-65_985-64del , LRG_750t1:c.985-65_985-64del	NP_109587.1:n.985-65_985-64del
XM_006722799.2:c.706-65_706-64del	XP_006722862.1:n.706-65_706-64del
XM_011528133.1:c.415-65_415-64del	XP_011526435.1:n.415-65_415-64del
XM_017026989.1:c.985-65_985-64del	XP_016882478.1:n.985-65_985-64del
XM_017026990.1:c.706-65_706-64del	XP_016882479.1:n.706-65_706-64del
NM_030662.4:c.985-65_985-64del MANE Select	NP_109587.1:n.985-65_985-64del