Canonical Allele Identifier: CA403381056
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090673T>A , CM000681.2:g.4090673T>A GRCh38
NC_000019.9:g.4090671T>A , CM000681.1:g.4090671T>A GRCh37
NC_000019.8:g.4041671T>A NCBI36
NG_007996.1:g.38456A>T , LRG_750:g.38456A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1567A>T
ENST00000688002.1:n.3279A>T
ENST00000688751.1:n.264A>T
ENST00000689792.1:n.1032A>T
ENST00000262948.10:c.1128A>T MANE Select ENSP00000262948.4:p.Glu376Asp
ENST00000262948.9:c.1128A>T ENSP00000262948.3:p.Glu376Asp
ENST00000394867.8:c.837A>T ENSP00000378336.1:p.Glu279Asp
ENST00000597263.5:n.313A>T
ENST00000599021.1:c.238A>T
ENST00000600584.5:n.2577A>T
ENST00000601786.5:n.1429A>T
NM_030662.3:c.1128A>T , LRG_750t1:c.1128A>T NP_109587.1:p.Glu376Asp
XM_006722799.2:c.849A>T XP_006722862.1:p.Glu283Asp
XM_011528133.1:c.558A>T XP_011526435.1:p.Glu186Asp
NM_030662.4:c.1128A>T MANE Select NP_109587.1:p.Glu376Asp