Canonical Allele Identifier: CA2319219769
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090655C= , CM000681.2:g.4090655C= GRCh38
NC_000019.9:g.4090653C= , CM000681.1:g.4090653C= GRCh37
NC_000019.8:g.4041653C= NCBI36
NG_007996.1:g.38474G= , LRG_750:g.38474G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1585G=
ENST00000688002.1:n.3297G=
ENST00000688751.1:n.282G=
ENST00000689792.1:n.1050G=
ENST00000262948.10:c.1146G= MANE Select ENSP00000262948.4:p.Trp382=
ENST00000262948.9:c.1146G= ENSP00000262948.3:p.Trp382=
ENST00000394867.8:c.855G= ENSP00000378336.1:p.Trp285=
ENST00000597263.5:n.331G=
ENST00000599021.1:c.256G=
ENST00000600584.5:n.2595G=
ENST00000601786.5:n.1447G=
NM_030662.3:c.1146G= , LRG_750t1:c.1146G= NP_109587.1:p.Trp382=
XM_006722799.2:c.867G= XP_006722862.1:p.Trp289=
XM_011528133.1:c.576G= XP_011526435.1:p.Trp192=
NM_030662.4:c.1146G= MANE Select NP_109587.1:p.Trp382=