Canonical Allele Identifier: CA403380770
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090629-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090629T>C , CM000681.2:g.4090629T>C GRCh38
NC_000019.9:g.4090627T>C , CM000681.1:g.4090627T>C GRCh37
NC_000019.8:g.4041627T>C NCBI36
NG_007996.1:g.38500A>G , LRG_750:g.38500A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1611A>G
ENST00000688002.1:n.3323A>G
ENST00000688751.1:n.308A>G
ENST00000689792.1:n.1076A>G
ENST00000262948.10:c.1172A>G MANE Select ENSP00000262948.4:p.Gln391Arg
ENST00000262948.9:c.1172A>G ENSP00000262948.3:p.Gln391Arg
ENST00000394867.8:c.881A>G ENSP00000378336.1:p.Gln294Arg
ENST00000597263.5:n.357A>G
ENST00000599021.1:c.282A>G
ENST00000600584.5:n.2621A>G
ENST00000601786.5:n.1473A>G
NM_030662.3:c.1172A>G , LRG_750t1:c.1172A>G NP_109587.1:p.Gln391Arg
XM_006722799.2:c.893A>G XP_006722862.1:p.Gln298Arg
XM_011528133.1:c.602A>G XP_011526435.1:p.Gln201Arg
NM_030662.4:c.1172A>G MANE Select NP_109587.1:p.Gln391Arg