Canonical Allele Identifier: CA2319219802
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090730G= , CM000681.2:g.4090730G= GRCh38
NC_000019.9:g.4090728G= , CM000681.1:g.4090728G= GRCh37
NC_000019.8:g.4041728G= NCBI36
NG_007996.1:g.38399C= , LRG_750:g.38399C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-22C=
ENST00000688002.1:n.3244-22C=
ENST00000688751.1:n.229-22C=
ENST00000689792.1:n.997-22C=
ENST00000262948.10:c.1093-22C= MANE Select ENSP00000262948.4:n.1093-22C=
ENST00000262948.9:c.1093-22C= ENSP00000262948.3:n.1093-22C=
ENST00000394867.8:c.802-22C= ENSP00000378336.1:n.802-22C=
ENST00000597263.5:n.278-22C=
ENST00000599021.1:c.203-22C=
ENST00000600584.5:n.2542-22C=
ENST00000601786.5:n.1394-22C=
NM_030662.3:c.1093-22C= , LRG_750t1:c.1093-22C= NP_109587.1:n.1093-22C=
XM_006722799.2:c.814-22C= XP_006722862.1:n.814-22C=
XM_011528133.1:c.523-22C= XP_011526435.1:n.523-22C=
NM_030662.4:c.1093-22C= MANE Select NP_109587.1:n.1093-22C=