Canonical Allele Identifier: CA2319221813

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094697_4094698delinsCA , CM000681.2:g.4094697_4094698delinsCA	GRCh38
NC_000019.9:g.4094695_4094696delinsCA , CM000681.1:g.4094695_4094696delinsCA	GRCh37
NC_000019.8:g.4045695_4045696delinsCA	NCBI36
NG_007996.1:g.34431_34432delinsTG , LRG_750:g.34431_34432delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-200_1486-199delinsTG
ENST00000688002.1:n.3198-200_3198-199delinsTG
ENST00000688751.1:n.183-200_183-199delinsTG
ENST00000689792.1:n.951-200_951-199delinsTG
ENST00000262948.10:c.1047-200_1047-199delinsTG MANE Select	ENSP00000262948.4:n.1047-200_1047-199delinsTG
ENST00000262948.9:c.1047-200_1047-199delinsTG	ENSP00000262948.3:n.1047-200_1047-199delinsTG
ENST00000394867.8:c.756-200_756-199delinsTG	ENSP00000378336.1:n.756-200_756-199delinsTG
ENST00000597263.5:n.232-200_232-199delinsTG
ENST00000599021.1:c.157-200_157-199delinsTG
ENST00000600584.5:n.2296_2297delinsTG
ENST00000601786.5:n.1348-200_1348-199delinsTG
NM_030662.3:c.1047-200_1047-199delinsTG , LRG_750t1:c.1047-200_1047-199delinsTG	NP_109587.1:n.1047-200_1047-199delinsTG
XM_006722799.2:c.768-200_768-199delinsTG	XP_006722862.1:n.768-200_768-199delinsTG
XM_011528133.1:c.477-200_477-199delinsTG	XP_011526435.1:n.477-200_477-199delinsTG
XM_017026989.1:c.1395_1396delinsTG	XP_016882478.1:p.Pro465=
XM_017026990.1:c.1116_1117delinsTG	XP_016882479.1:p.Pro372=
NM_030662.4:c.1047-200_1047-199delinsTG MANE Select	NP_109587.1:n.1047-200_1047-199delinsTG