Canonical Allele Identifier: CA2319219699
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090545T= , CM000681.2:g.4090545T= GRCh38
NC_000019.9:g.4090543T= , CM000681.1:g.4090543T= GRCh37
NC_000019.8:g.4041543T= NCBI36
NG_007996.1:g.38584A= , LRG_750:g.38584A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1695A=
ENST00000688002.1:n.3407A=
ENST00000688751.1:n.392A=
ENST00000689792.1:n.1160A=
ENST00000262948.10:c.*53A= MANE Select ENSP00000262948.4:n.*53A=
ENST00000262948.9:c.*53A= ENSP00000262948.3:n.*53A=
ENST00000394867.8:c.*53A= ENSP00000378336.1:n.*53A=
ENST00000597263.5:n.441A=
ENST00000600584.5:n.2705A=
ENST00000601786.5:n.1557A=
NM_030662.3:c.*53A= , LRG_750t1:c.*53A= NP_109587.1:n.*53A=
XM_006722799.2:c.*53A= XP_006722862.1:n.*53A=
XM_011528133.1:c.*53A= XP_011526435.1:n.*53A=
NM_030662.4:c.*53A= MANE Select NP_109587.1:n.*53A=