Canonical Allele Identifier: CA403381061
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090675C>A , CM000681.2:g.4090675C>A GRCh38
NC_000019.9:g.4090673C>A , CM000681.1:g.4090673C>A GRCh37
NC_000019.8:g.4041673C>A NCBI36
NG_007996.1:g.38454G>T , LRG_750:g.38454G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1565G>T
ENST00000688002.1:n.3277G>T
ENST00000688751.1:n.262G>T
ENST00000689792.1:n.1030G>T
ENST00000262948.10:c.1126G>T MANE Select ENSP00000262948.4:p.Glu376Ter
ENST00000262948.9:c.1126G>T ENSP00000262948.3:p.Glu376Ter
ENST00000394867.8:c.835G>T ENSP00000378336.1:p.Glu279Ter
ENST00000597263.5:n.311G>T
ENST00000599021.1:c.236G>T
ENST00000600584.5:n.2575G>T
ENST00000601786.5:n.1427G>T
NM_030662.3:c.1126G>T , LRG_750t1:c.1126G>T NP_109587.1:p.Glu376Ter
XM_006722799.2:c.847G>T XP_006722862.1:p.Glu283Ter
XM_011528133.1:c.556G>T XP_011526435.1:p.Glu186Ter
NM_030662.4:c.1126G>T MANE Select NP_109587.1:p.Glu376Ter