Canonical Allele Identifier: CA2319221782

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094630_4094632delinsGCA , CM000681.2:g.4094630_4094632delinsGCA	GRCh38
NC_000019.9:g.4094628_4094630delinsGCA , CM000681.1:g.4094628_4094630delinsGCA	GRCh37
NC_000019.8:g.4045628_4045630delinsGCA	NCBI36
NG_007996.1:g.34497_34499delinsTGC , LRG_750:g.34497_34499delinsTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-134_1486-132delinsTGC
ENST00000688002.1:n.3198-134_3198-132delinsTGC
ENST00000688751.1:n.183-134_183-132delinsTGC
ENST00000689792.1:n.951-134_951-132delinsTGC
ENST00000262948.10:c.1047-134_1047-132delinsTGC MANE Select	ENSP00000262948.4:n.1047-134_1047-132delinsTGC
ENST00000262948.9:c.1047-134_1047-132delinsTGC	ENSP00000262948.3:n.1047-134_1047-132delinsTGC
ENST00000394867.8:c.756-134_756-132delinsTGC	ENSP00000378336.1:n.756-134_756-132delinsTGC
ENST00000597263.5:n.232-134_232-132delinsTGC
ENST00000599021.1:c.157-134_157-132delinsTGC
ENST00000600584.5:n.2362_2364delinsTGC
ENST00000601786.5:n.1348-134_1348-132delinsTGC
NM_030662.3:c.1047-134_1047-132delinsTGC , LRG_750t1:c.1047-134_1047-132delinsTGC	NP_109587.1:n.1047-134_1047-132delinsTGC
XM_006722799.2:c.768-134_768-132delinsTGC	XP_006722862.1:n.768-134_768-132delinsTGC
XM_011528133.1:c.477-134_477-132delinsTGC	XP_011526435.1:n.477-134_477-132delinsTGC
XM_017026989.1:c.1461_1463delinsTGC	XP_016882478.1:p.Cys487=
XM_017026990.1:c.1182_1184delinsTGC	XP_016882479.1:p.Cys394=
NM_030662.4:c.1047-134_1047-132delinsTGC MANE Select	NP_109587.1:n.1047-134_1047-132delinsTGC