Canonical Allele Identifier: CA2955275380

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117464dup , CM000681.2:g.4117464dup	GRCh38
NC_000019.9:g.4117462dup , CM000681.1:g.4117462dup	GRCh37
NC_000019.8:g.4068462dup	NCBI36
NG_007996.1:g.11665dup , LRG_750:g.11665dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.697dup
ENST00000687128.1:n.697dup
ENST00000262948.10:c.258dup MANE Select	ENSP00000262948.4:p.Thr87HisfsTer20
ENST00000262948.9:c.258dup	ENSP00000262948.3:p.Thr87HisfsTer20
ENST00000394867.8:c.-34dup	ENSP00000378336.1:n.-34dup
ENST00000599345.1:n.455dup
NM_030662.3:c.258dup , LRG_750t1:c.258dup	NP_109587.1:p.Thr87HisfsTer20
XM_006722799.2:c.258dup	XP_006722862.1:p.Thr87HisfsTer20
XM_017026989.1:c.258dup	XP_016882478.1:p.Thr87HisfsTer20
XM_017026990.1:c.258dup	XP_016882479.1:p.Thr87HisfsTer20
XM_017026991.1:c.258dup	XP_016882480.1:p.Thr87HisfsTer20
NM_030662.4:c.258dup MANE Select	NP_109587.1:p.Thr87HisfsTer20