Canonical Allele Identifier: CA2319219764
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090643G= , CM000681.2:g.4090643G= GRCh38
NC_000019.9:g.4090641G= , CM000681.1:g.4090641G= GRCh37
NC_000019.8:g.4041641G= NCBI36
NG_007996.1:g.38486C= , LRG_750:g.38486C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1597C=
ENST00000688002.1:n.3309C=
ENST00000688751.1:n.294C=
ENST00000689792.1:n.1062C=
ENST00000262948.10:c.1158C= MANE Select ENSP00000262948.4:p.Thr386=
ENST00000262948.9:c.1158C= ENSP00000262948.3:p.Thr386=
ENST00000394867.8:c.867C= ENSP00000378336.1:p.Thr289=
ENST00000597263.5:n.343C=
ENST00000599021.1:c.268C=
ENST00000600584.5:n.2607C=
ENST00000601786.5:n.1459C=
NM_030662.3:c.1158C= , LRG_750t1:c.1158C= NP_109587.1:p.Thr386=
XM_006722799.2:c.879C= XP_006722862.1:p.Thr293=
XM_011528133.1:c.588C= XP_011526435.1:p.Thr196=
NM_030662.4:c.1158C= MANE Select NP_109587.1:p.Thr386=