Canonical Allele Identifier: CA2536026307

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095300_4095308dup , CM000681.2:g.4095300_4095308dup	GRCh38
NC_000019.9:g.4095298_4095306dup , CM000681.1:g.4095298_4095306dup	GRCh37
NC_000019.8:g.4046298_4046306dup	NCBI36
NG_007996.1:g.33826_33834dup , LRG_750:g.33826_33834dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1485+85_1485+93dup
ENST00000688002.1:n.3197+85_3197+93dup
ENST00000688751.1:n.182+85_182+93dup
ENST00000689792.1:n.950+85_950+93dup
ENST00000262948.10:c.1046+85_1046+93dup MANE Select	ENSP00000262948.4:n.1046+85_1046+93dup
ENST00000262948.9:c.1046+85_1046+93dup	ENSP00000262948.3:n.1046+85_1046+93dup
ENST00000394867.8:c.755+85_755+93dup	ENSP00000378336.1:n.755+85_755+93dup
ENST00000597263.5:n.231+85_231+93dup
ENST00000599021.1:c.156+85_156+93dup
ENST00000600584.5:n.1691_1699dup
ENST00000601786.5:n.1347+85_1347+93dup
NM_030662.3:c.1046+85_1046+93dup , LRG_750t1:c.1046+85_1046+93dup	NP_109587.1:n.1046+85_1046+93dup
XM_006722799.2:c.767+85_767+93dup	XP_006722862.1:n.767+85_767+93dup
XM_011528133.1:c.476+85_476+93dup	XP_011526435.1:n.476+85_476+93dup
XM_017026989.1:c.1046+85_1046+93dup	XP_016882478.1:n.1046+85_1046+93dup
XM_017026990.1:c.767+85_767+93dup	XP_016882479.1:n.767+85_767+93dup
NM_030662.4:c.1046+85_1046+93dup MANE Select	NP_109587.1:n.1046+85_1046+93dup