Canonical Allele Identifier: CA2319219767
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090652C= , CM000681.2:g.4090652C= GRCh38
NC_000019.9:g.4090650C= , CM000681.1:g.4090650C= GRCh37
NC_000019.8:g.4041650C= NCBI36
NG_007996.1:g.38477G= , LRG_750:g.38477G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1588G=
ENST00000688002.1:n.3300G=
ENST00000688751.1:n.285G=
ENST00000689792.1:n.1053G=
ENST00000262948.10:c.1149G= MANE Select ENSP00000262948.4:p.Leu383=
ENST00000262948.9:c.1149G= ENSP00000262948.3:p.Leu383=
ENST00000394867.8:c.858G= ENSP00000378336.1:p.Leu286=
ENST00000597263.5:n.334G=
ENST00000599021.1:c.259G=
ENST00000600584.5:n.2598G=
ENST00000601786.5:n.1450G=
NM_030662.3:c.1149G= , LRG_750t1:c.1149G= NP_109587.1:p.Leu383=
XM_006722799.2:c.870G= XP_006722862.1:p.Leu290=
XM_011528133.1:c.579G= XP_011526435.1:p.Leu193=
NM_030662.4:c.1149G= MANE Select NP_109587.1:p.Leu383=