Canonical Allele Identifier: CA2319221564

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094243_4094244delinsCT , CM000681.2:g.4094243_4094244delinsCT	GRCh38
NC_000019.9:g.4094241_4094242delinsCT , CM000681.1:g.4094241_4094242delinsCT	GRCh37
NC_000019.8:g.4045241_4045242delinsCT	NCBI36
NG_007996.1:g.34885_34886delinsAG , LRG_750:g.34885_34886delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1531+209_1531+210delinsAG
ENST00000688002.1:n.3243+209_3243+210delinsAG
ENST00000688751.1:n.228+209_228+210delinsAG
ENST00000689792.1:n.996+209_996+210delinsAG
ENST00000262948.10:c.1092+209_1092+210delinsAG MANE Select	ENSP00000262948.4:n.1092+209_1092+210delinsAG
ENST00000262948.9:c.1092+209_1092+210delinsAG	ENSP00000262948.3:n.1092+209_1092+210delinsAG
ENST00000394867.8:c.801+209_801+210delinsAG	ENSP00000378336.1:n.801+209_801+210delinsAG
ENST00000597263.5:n.277+209_277+210delinsAG
ENST00000599021.1:c.202+209_202+210delinsAG
ENST00000600584.5:n.2541+209_2541+210delinsAG
ENST00000601786.5:n.1393+209_1393+210delinsAG
NM_030662.3:c.1092+209_1092+210delinsAG , LRG_750t1:c.1092+209_1092+210delinsAG	NP_109587.1:n.1092+209_1092+210delinsAG
XM_006722799.2:c.813+209_813+210delinsAG	XP_006722862.1:n.813+209_813+210delinsAG
XM_011528133.1:c.522+209_522+210delinsAG	XP_011526435.1:n.522+209_522+210delinsAG
NM_030662.4:c.1092+209_1092+210delinsAG MANE Select	NP_109587.1:n.1092+209_1092+210delinsAG