Canonical Allele Identifier: CA2319219703
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090555C= , CM000681.2:g.4090555C= GRCh38
NC_000019.9:g.4090553C= , CM000681.1:g.4090553C= GRCh37
NC_000019.8:g.4041553C= NCBI36
NG_007996.1:g.38574G= , LRG_750:g.38574G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1685G=
ENST00000688002.1:n.3397G=
ENST00000688751.1:n.382G=
ENST00000689792.1:n.1150G=
ENST00000262948.10:c.*43G= MANE Select ENSP00000262948.4:n.*43G=
ENST00000262948.9:c.*43G= ENSP00000262948.3:n.*43G=
ENST00000394867.8:c.*43G= ENSP00000378336.1:n.*43G=
ENST00000597263.5:n.431G=
ENST00000600584.5:n.2695G=
ENST00000601786.5:n.1547G=
NM_030662.3:c.*43G= , LRG_750t1:c.*43G= NP_109587.1:n.*43G=
XM_006722799.2:c.*43G= XP_006722862.1:n.*43G=
XM_011528133.1:c.*43G= XP_011526435.1:n.*43G=
NM_030662.4:c.*43G= MANE Select NP_109587.1:n.*43G=