Canonical Allele Identifier: CA2319219695
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090538C= , CM000681.2:g.4090538C= GRCh38
NC_000019.9:g.4090536C= , CM000681.1:g.4090536C= GRCh37
NC_000019.8:g.4041536C= NCBI36
NG_007996.1:g.38591G= , LRG_750:g.38591G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1702G=
ENST00000688002.1:n.3414G=
ENST00000688751.1:n.399G=
ENST00000689792.1:n.1167G=
ENST00000262948.10:c.*60G= MANE Select ENSP00000262948.4:n.*60G=
ENST00000262948.9:c.*60G= ENSP00000262948.3:n.*60G=
ENST00000394867.8:c.*60G= ENSP00000378336.1:n.*60G=
ENST00000597263.5:n.448G=
ENST00000600584.5:n.2712G=
ENST00000601786.5:n.1564G=
NM_030662.3:c.*60G= , LRG_750t1:c.*60G= NP_109587.1:n.*60G=
XM_006722799.2:c.*60G= XP_006722862.1:n.*60G=
XM_011528133.1:c.*60G= XP_011526435.1:n.*60G=
NM_030662.4:c.*60G= MANE Select NP_109587.1:n.*60G=