Canonical Allele Identifier: CA2319219595
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090397C= , CM000681.2:g.4090397C= GRCh38
NC_000019.9:g.4090395C= , CM000681.1:g.4090395C= GRCh37
NC_000019.8:g.4041395C= NCBI36
NG_007996.1:g.38732G= , LRG_750:g.38732G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1843G=
ENST00000688751.1:n.540G=
ENST00000689792.1:n.1308G=
ENST00000262948.10:c.*201G= MANE Select ENSP00000262948.4:n.*201G=
ENST00000262948.9:c.*201G= ENSP00000262948.3:n.*201G=
ENST00000394867.8:c.*201G= ENSP00000378336.1:n.*201G=
ENST00000600584.5:n.2853G=
ENST00000601786.5:n.1705G=
NM_030662.3:c.*201G= , LRG_750t1:c.*201G= NP_109587.1:n.*201G=
XM_006722799.2:c.*201G= XP_006722862.1:n.*201G=
XM_011528133.1:c.*201G= XP_011526435.1:n.*201G=
NM_030662.4:c.*201G= MANE Select NP_109587.1:n.*201G=