Canonical Allele Identifier: CA2319219713
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090573C= , CM000681.2:g.4090573C= GRCh38
NC_000019.9:g.4090571C= , CM000681.1:g.4090571C= GRCh37
NC_000019.8:g.4041571C= NCBI36
NG_007996.1:g.38556G= , LRG_750:g.38556G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1667G=
ENST00000688002.1:n.3379G=
ENST00000688751.1:n.364G=
ENST00000689792.1:n.1132G=
ENST00000262948.10:c.*25G= MANE Select ENSP00000262948.4:n.*25G=
ENST00000262948.9:c.*25G= ENSP00000262948.3:n.*25G=
ENST00000394867.8:c.*25G= ENSP00000378336.1:n.*25G=
ENST00000597263.5:n.413G=
ENST00000600584.5:n.2677G=
ENST00000601786.5:n.1529G=
NM_030662.3:c.*25G= , LRG_750t1:c.*25G= NP_109587.1:n.*25G=
XM_006722799.2:c.*25G= XP_006722862.1:n.*25G=
XM_011528133.1:c.*25G= XP_011526435.1:n.*25G=
NM_030662.4:c.*25G= MANE Select NP_109587.1:n.*25G=