Canonical Allele Identifier: CA2319219744
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090614G= , CM000681.2:g.4090614G= GRCh38
NC_000019.9:g.4090612G= , CM000681.1:g.4090612G= GRCh37
NC_000019.8:g.4041612G= NCBI36
NG_007996.1:g.38515C= , LRG_750:g.38515C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1626C=
ENST00000688002.1:n.3338C=
ENST00000688751.1:n.323C=
ENST00000689792.1:n.1091C=
ENST00000262948.10:c.1187C= MANE Select ENSP00000262948.4:p.Thr396=
ENST00000262948.9:c.1187C= ENSP00000262948.3:p.Thr396=
ENST00000394867.8:c.896C= ENSP00000378336.1:p.Thr299=
ENST00000597263.5:n.372C=
ENST00000599021.1:c.297C=
ENST00000600584.5:n.2636C=
ENST00000601786.5:n.1488C=
NM_030662.3:c.1187C= , LRG_750t1:c.1187C= NP_109587.1:p.Thr396=
XM_006722799.2:c.908C= XP_006722862.1:p.Thr303=
XM_011528133.1:c.617C= XP_011526435.1:p.Thr206=
NM_030662.4:c.1187C= MANE Select NP_109587.1:p.Thr396=