Canonical Allele Identifier: CA2319219750
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090620G= , CM000681.2:g.4090620G= GRCh38
NC_000019.9:g.4090618G= , CM000681.1:g.4090618G= GRCh37
NC_000019.8:g.4041618G= NCBI36
NG_007996.1:g.38509C= , LRG_750:g.38509C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1620C=
ENST00000688002.1:n.3332C=
ENST00000688751.1:n.317C=
ENST00000689792.1:n.1085C=
ENST00000262948.10:c.1181C= MANE Select ENSP00000262948.4:p.Thr394=
ENST00000262948.9:c.1181C= ENSP00000262948.3:p.Thr394=
ENST00000394867.8:c.890C= ENSP00000378336.1:p.Thr297=
ENST00000597263.5:n.366C=
ENST00000599021.1:c.291C=
ENST00000600584.5:n.2630C=
ENST00000601786.5:n.1482C=
NM_030662.3:c.1181C= , LRG_750t1:c.1181C= NP_109587.1:p.Thr394=
XM_006722799.2:c.902C= XP_006722862.1:p.Thr301=
XM_011528133.1:c.611C= XP_011526435.1:p.Thr204=
NM_030662.4:c.1181C= MANE Select NP_109587.1:p.Thr394=