Canonical Allele Identifier: CA403392868
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs2145080710
COSMIC: COSM327847

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4117589C>T , CM000681.2:g.4117589C>T GRCh38
NC_000019.9:g.4117587C>T , CM000681.1:g.4117587C>T GRCh37
NC_000019.8:g.4068587C>T NCBI36
NG_007996.1:g.11540G>A , LRG_750:g.11540G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000394867.9:n.572G>A
ENST00000687128.1:n.572G>A
ENST00000262948.10:c.133G>A MANE Select ENSP00000262948.4:p.Glu45Lys
ENST00000262948.9:c.133G>A ENSP00000262948.3:p.Glu45Lys
ENST00000394867.8:c.-159G>A ENSP00000378336.1:n.-159G>A
ENST00000599345.1:n.330G>A
NM_030662.3:c.133G>A , LRG_750t1:c.133G>A NP_109587.1:p.Glu45Lys
XM_006722799.2:c.133G>A XP_006722862.1:p.Glu45Lys
XM_017026989.1:c.133G>A XP_016882478.1:p.Glu45Lys
XM_017026990.1:c.133G>A XP_016882479.1:p.Glu45Lys
XM_017026991.1:c.133G>A XP_016882480.1:p.Glu45Lys
NM_030662.4:c.133G>A MANE Select NP_109587.1:p.Glu45Lys