Canonical Allele Identifier: CA2319219578
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090366A= , CM000681.2:g.4090366A= GRCh38
NC_000019.9:g.4090364A= , CM000681.1:g.4090364A= GRCh37
NC_000019.8:g.4041364A= NCBI36
NG_007996.1:g.38763T= , LRG_750:g.38763T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1874T=
ENST00000688751.1:n.571T=
ENST00000689792.1:n.1339T=
ENST00000262948.10:c.*232T= MANE Select ENSP00000262948.4:n.*232T=
ENST00000262948.9:c.*232T= ENSP00000262948.3:n.*232T=
ENST00000394867.8:c.*232T= ENSP00000378336.1:n.*232T=
ENST00000600584.5:n.2884T=
ENST00000601786.5:n.1736T=
NM_030662.3:c.*232T= , LRG_750t1:c.*232T= NP_109587.1:n.*232T=
XM_006722799.2:c.*232T= XP_006722862.1:n.*232T=
XM_011528133.1:c.*232T= XP_011526435.1:n.*232T=
NM_030662.4:c.*232T= MANE Select NP_109587.1:n.*232T=