Canonical Allele Identifier: CA504984312
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs1186326424
gnomAD v2: 19-4090626-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090628C>T , CM000681.2:g.4090628C>T GRCh38
NC_000019.9:g.4090626C>T , CM000681.1:g.4090626C>T GRCh37
NC_000019.8:g.4041626C>T NCBI36
NG_007996.1:g.38501G>A , LRG_750:g.38501G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1612G>A
ENST00000688002.1:n.3324G>A
ENST00000688751.1:n.309G>A
ENST00000689792.1:n.1077G>A
ENST00000262948.10:c.1173G>A MANE Select ENSP00000262948.4:p.Gln391=
ENST00000262948.9:c.1173G>A ENSP00000262948.3:p.Gln391=
ENST00000394867.8:c.882G>A ENSP00000378336.1:p.Gln294=
ENST00000597263.5:n.358G>A
ENST00000599021.1:c.283G>A
ENST00000600584.5:n.2622G>A
ENST00000601786.5:n.1474G>A
NM_030662.3:c.1173G>A , LRG_750t1:c.1173G>A NP_109587.1:p.Gln391=
XM_006722799.2:c.894G>A XP_006722862.1:p.Gln298=
XM_011528133.1:c.603G>A XP_011526435.1:p.Gln201=
NM_030662.4:c.1173G>A MANE Select NP_109587.1:p.Gln391=