Canonical Allele Identifier: CA2319219586
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090382C= , CM000681.2:g.4090382C= GRCh38
NC_000019.9:g.4090380C= , CM000681.1:g.4090380C= GRCh37
NC_000019.8:g.4041380C= NCBI36
NG_007996.1:g.38747G= , LRG_750:g.38747G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1858G=
ENST00000688751.1:n.555G=
ENST00000689792.1:n.1323G=
ENST00000262948.10:c.*216G= MANE Select ENSP00000262948.4:n.*216G=
ENST00000262948.9:c.*216G= ENSP00000262948.3:n.*216G=
ENST00000394867.8:c.*216G= ENSP00000378336.1:n.*216G=
ENST00000600584.5:n.2868G=
ENST00000601786.5:n.1720G=
NM_030662.3:c.*216G= , LRG_750t1:c.*216G= NP_109587.1:n.*216G=
XM_006722799.2:c.*216G= XP_006722862.1:n.*216G=
XM_011528133.1:c.*216G= XP_011526435.1:n.*216G=
NM_030662.4:c.*216G= MANE Select NP_109587.1:n.*216G=