Canonical Allele Identifier: CA2319224381

Gene: MAP2K2

Linked Data

• dbSNP Id: rs763469132

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099259_4099261dup , CM000681.2:g.4099259_4099261dup	GRCh38
NC_000019.9:g.4099257_4099259dup , CM000681.1:g.4099257_4099259dup	GRCh37
NC_000019.8:g.4050257_4050259dup	NCBI36
NG_007996.1:g.29872_29874dup , LRG_750:g.29872_29874dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1302_1304dup
ENST00000687128.1:n.1302_1304dup
ENST00000688002.1:n.1157_1159dup
ENST00000689792.1:n.767_769dup
ENST00000262948.10:c.863_865dup MANE Select	ENSP00000262948.4:p.Glu288_Gly289insGlu
ENST00000262948.9:c.863_865dup	ENSP00000262948.3:p.Glu288_Gly289insGlu
ENST00000394867.8:c.572_574dup	ENSP00000378336.1:p.Glu191_Gly192insGlu
ENST00000593364.5:n.810_812dup
ENST00000595715.1:n.678_680dup
ENST00000597263.5:n.169+1762_169+1764dup
ENST00000599021.1:c.29+1762_29+1764dup
ENST00000600584.5:n.1423_1425dup
ENST00000601786.5:n.1164_1166dup
NM_030662.3:c.863_865dup , LRG_750t1:c.863_865dup	NP_109587.1:p.Glu288_Gly289insGlu
XM_006722799.2:c.705+1762_705+1764dup	XP_006722862.1:n.705+1762_705+1764dup
XM_011528133.1:c.293_295dup	XP_011526435.1:p.Glu98_Gly99insGlu
XM_017026989.1:c.863_865dup	XP_016882478.1:p.Glu288_Gly289insGlu
XM_017026990.1:c.705+1762_705+1764dup	XP_016882479.1:n.705+1762_705+1764dup
NM_030662.4:c.863_865dup MANE Select	NP_109587.1:p.Glu288_Gly289insGlu