Canonical Allele Identifier: CA2319219574
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090355T= , CM000681.2:g.4090355T= GRCh38
NC_000019.9:g.4090353T= , CM000681.1:g.4090353T= GRCh37
NC_000019.8:g.4041353T= NCBI36
NG_007996.1:g.38774A= , LRG_750:g.38774A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1885A=
ENST00000688751.1:n.582A=
ENST00000689792.1:n.1350A=
ENST00000262948.10:c.*243A= MANE Select ENSP00000262948.4:n.*243A=
ENST00000262948.9:c.*243A= ENSP00000262948.3:n.*243A=
ENST00000394867.8:c.*243A= ENSP00000378336.1:n.*243A=
ENST00000600584.5:n.2895A=
ENST00000601786.5:n.1747A=
NM_030662.3:c.*243A= , LRG_750t1:c.*243A= NP_109587.1:n.*243A=
XM_006722799.2:c.*243A= XP_006722862.1:n.*243A=
XM_011528133.1:c.*243A= XP_011526435.1:n.*243A=
NM_030662.4:c.*243A= MANE Select NP_109587.1:n.*243A=