Canonical Allele Identifier: CA2319219783
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090685G= , CM000681.2:g.4090685G= GRCh38
NC_000019.9:g.4090683G= , CM000681.1:g.4090683G= GRCh37
NC_000019.8:g.4041683G= NCBI36
NG_007996.1:g.38444C= , LRG_750:g.38444C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1555C=
ENST00000688002.1:n.3267C=
ENST00000688751.1:n.252C=
ENST00000689792.1:n.1020C=
ENST00000262948.10:c.1116C= MANE Select ENSP00000262948.4:p.Ser372=
ENST00000262948.9:c.1116C= ENSP00000262948.3:p.Ser372=
ENST00000394867.8:c.825C= ENSP00000378336.1:p.Ser275=
ENST00000597263.5:n.301C=
ENST00000599021.1:c.226C=
ENST00000600584.5:n.2565C=
ENST00000601786.5:n.1417C=
NM_030662.3:c.1116C= , LRG_750t1:c.1116C= NP_109587.1:p.Ser372=
XM_006722799.2:c.837C= XP_006722862.1:p.Ser279=
XM_011528133.1:c.546C= XP_011526435.1:p.Ser182=
NM_030662.4:c.1116C= MANE Select NP_109587.1:p.Ser372=