Canonical Allele Identifier: CA403380777
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090630G>A , CM000681.2:g.4090630G>A GRCh38
NC_000019.9:g.4090628G>A , CM000681.1:g.4090628G>A GRCh37
NC_000019.8:g.4041628G>A NCBI36
NG_007996.1:g.38499C>T , LRG_750:g.38499C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1610C>T
ENST00000688002.1:n.3322C>T
ENST00000688751.1:n.307C>T
ENST00000689792.1:n.1075C>T
ENST00000262948.10:c.1171C>T MANE Select ENSP00000262948.4:p.Gln391Ter
ENST00000262948.9:c.1171C>T ENSP00000262948.3:p.Gln391Ter
ENST00000394867.8:c.880C>T ENSP00000378336.1:p.Gln294Ter
ENST00000597263.5:n.356C>T
ENST00000599021.1:c.281C>T
ENST00000600584.5:n.2620C>T
ENST00000601786.5:n.1472C>T
NM_030662.3:c.1171C>T , LRG_750t1:c.1171C>T NP_109587.1:p.Gln391Ter
XM_006722799.2:c.892C>T XP_006722862.1:p.Gln298Ter
XM_011528133.1:c.601C>T XP_011526435.1:p.Gln201Ter
NM_030662.4:c.1171C>T MANE Select NP_109587.1:p.Gln391Ter