Canonical Allele Identifier: CA2319219737

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090606_4090609delinsCGGT , CM000681.2:g.4090606_4090609delinsCGGT	GRCh38
NC_000019.9:g.4090604_4090607delinsCGGT , CM000681.1:g.4090604_4090607delinsCGGT	GRCh37
NC_000019.8:g.4041604_4041607delinsCGGT	NCBI36
NG_007996.1:g.38520_38523delinsACCG , LRG_750:g.38520_38523delinsACCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1631_1634delinsACCG
ENST00000688002.1:n.3343_3346delinsACCG
ENST00000688751.1:n.328_331delinsACCG
ENST00000689792.1:n.1096_1099delinsACCG
ENST00000262948.10:c.1192_1195delinsACCG MANE Select	ENSP00000262948.4:p.Thr398=
ENST00000262948.9:c.1192_1195delinsACCG	ENSP00000262948.3:p.Thr398=
ENST00000394867.8:c.901_904delinsACCG	ENSP00000378336.1:p.Thr301=
ENST00000597263.5:n.377_380delinsACCG
ENST00000599021.1:c.302_305delinsACCG
ENST00000600584.5:n.2641_2644delinsACCG
ENST00000601786.5:n.1493_1496delinsACCG
NM_030662.3:c.1192_1195delinsACCG , LRG_750t1:c.1192_1195delinsACCG	NP_109587.1:p.Thr398=
XM_006722799.2:c.913_916delinsACCG	XP_006722862.1:p.Thr305=
XM_011528133.1:c.622_625delinsACCG	XP_011526435.1:p.Thr208=
NM_030662.4:c.1192_1195delinsACCG MANE Select	NP_109587.1:p.Thr398=