Canonical Allele Identifier: CA16043144
Gene: DYRK1A HGNC NCBI

Linked Data

ClinVar Variation Id: 373087
dbSNP Id: rs1057518204

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.37480659C>T , CM000683.2:g.37480659C>T GRCh38
NC_000021.8:g.38852961C>T , CM000683.1:g.38852961C>T GRCh37
NC_000021.7:g.37774831C>T NCBI36
NG_009366.1:g.118103C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000338785.8:c.349C>T ENSP00000342690.3:p.Arg117Ter
ENST00000398960.7:c.349C>T ENSP00000381932.2:p.Arg117Ter
ENST00000426672.6:c.349C>T ENSP00000412269.2:p.Arg117Ter
ENST00000462274.2:n.243C>T
ENST00000642309.1:c.235C>T ENSP00000495596.1:p.Arg79Ter
ENST00000643355.1:n.38C>T
ENST00000643551.1:c.322C>T ENSP00000494698.1:p.Arg108Ter
ENST00000643624.1:c.322C>T ENSP00000493627.1:p.Arg108Ter
ENST00000643854.1:c.235C>T ENSP00000493653.1:p.Arg79Ter
ENST00000644942.1:c.349C>T ENSP00000494544.1:p.Arg117Ter
ENST00000645424.1:c.349C>T ENSP00000494897.1:p.Arg117Ter
ENST00000645774.1:c.370C>T ENSP00000494536.1:p.Arg124Ter
ENST00000646523.1:c.349C>T ENSP00000495632.1:p.Arg117Ter
ENST00000646548.1:c.322C>T ENSP00000495908.1:p.Arg108Ter
ENST00000647188.2:c.322C>T MANE Select ENSP00000494572.1:p.Arg108Ter
ENST00000647425.1:c.322C>T ENSP00000496748.1:p.Arg108Ter
ENST00000647504.1:c.235C>T ENSP00000495571.1:p.Arg79Ter
ENST00000338785.7:c.349C>T ENSP00000342690.3:p.Arg117Ter
ENST00000339659.8:c.322C>T ENSP00000340373.3:p.Arg108Ter
ENST00000398956.2:c.349C>T ENSP00000381929.2:p.Arg117Ter
ENST00000398960.6:c.349C>T ENSP00000381932.2:p.Arg117Ter
ENST00000426672.5:c.349C>T ENSP00000412269.1:p.Arg117Ter
ENST00000462274.1:n.1007C>T
NM_001396.3:c.349C>T NP_001387.2:p.Arg117Ter
NM_101395.2:c.349C>T NP_567824.1:p.Arg117Ter
NM_130436.2:c.322C>T NP_569120.1:p.Arg108Ter
NM_130438.2:c.349C>T NP_569122.1:p.Arg117Ter
XM_005260931.3:c.262C>T XP_005260988.1:p.Arg88Ter
XM_006723976.2:c.349C>T XP_006724039.1:p.Arg117Ter
XM_006723977.2:c.349C>T XP_006724040.1:p.Arg117Ter
XM_006723978.2:c.349C>T XP_006724041.1:p.Arg117Ter
XM_006723979.2:c.322C>T XP_006724042.1:p.Arg108Ter
XM_011529482.1:c.370C>T XP_011527784.1:p.Arg124Ter
XM_011529483.1:c.349C>T XP_011527785.1:p.Arg117Ter
XM_011529484.1:c.343C>T XP_011527786.1:p.Arg115Ter
XM_011529485.1:c.235C>T XP_011527787.1:p.Arg79Ter
XR_937703.1:n.707-1543G>A
XR_937704.1:n.618-1543G>A
NM_001347721.1:c.322C>T NP_001334650.1:p.Arg108Ter
NM_001347722.1:c.322C>T NP_001334651.1:p.Arg108Ter
NM_001347723.1:c.235C>T NP_001334652.1:p.Arg79Ter
NM_001396.4:c.349C>T NP_001387.2:p.Arg117Ter
XM_006723976.3:c.349C>T XP_006724039.1:p.Arg117Ter
XM_006723977.3:c.349C>T XP_006724040.1:p.Arg117Ter
XM_006723978.3:c.349C>T XP_006724041.1:p.Arg117Ter
XM_011529483.2:c.349C>T XP_011527785.1:p.Arg117Ter
XM_017028284.1:c.322C>T XP_016883773.1:p.Arg108Ter
XM_017028286.2:c.262C>T XP_016883775.1:p.Arg88Ter
XM_024452057.1:c.235C>T XP_024307825.1:p.Arg79Ter
XR_001755034.1:n.139-1543G>A
NM_001347721.2:c.322C>T MANE Select NP_001334650.1:p.Arg108Ter
NM_001347722.2:c.322C>T NP_001334651.1:p.Arg108Ter
NM_001347723.2:c.235C>T NP_001334652.1:p.Arg79Ter
NM_001396.5:c.349C>T NP_001387.2:p.Arg117Ter