Canonical Allele Identifier: CA16044386
Gene: DYRK1A HGNC NCBI

Linked Data

ClinVar Variation Id: 375618
ClinVar RCV Id: RCV000417097
dbSNP Id: rs1057519402

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.37478270_37478274del , CM000683.2:g.37478270_37478274del GRCh38
NC_000021.8:g.38850572_38850576del , CM000683.1:g.38850572_38850576del GRCh37
NC_000021.7:g.37772442_37772446del NCBI36
NG_009366.1:g.115714_115718del

Transcript Alleles

HGVS Amino-acid change
ENST00000338785.8:c.297_301del ENSP00000342690.3:p.Leu100GlnfsTer7
ENST00000398960.7:c.297_301del ENSP00000381932.2:p.Leu100GlnfsTer7
ENST00000426672.6:c.297_301del ENSP00000412269.2:p.Leu100GlnfsTer7
ENST00000462274.2:n.191_195del
ENST00000642309.1:c.183_187del ENSP00000495596.1:p.Leu62GlnfsTer7
ENST00000643551.1:c.270_274del ENSP00000494698.1:p.Leu91GlnfsTer7
ENST00000643624.1:c.270_274del ENSP00000493627.1:p.Leu91GlnfsTer7
ENST00000643854.1:c.183_187del ENSP00000493653.1:p.Leu62GlnfsTer7
ENST00000644942.1:c.297_301del ENSP00000494544.1:p.Leu100GlnfsTer7
ENST00000645424.1:c.297_301del ENSP00000494897.1:p.Leu100GlnfsTer7
ENST00000645774.1:c.318_322del ENSP00000494536.1:p.Leu107GlnfsTer7
ENST00000646523.1:c.297_301del ENSP00000495632.1:p.Leu100GlnfsTer7
ENST00000646548.1:c.270_274del ENSP00000495908.1:p.Leu91GlnfsTer7
ENST00000647188.2:c.270_274del MANE Select ENSP00000494572.1:p.Leu91GlnfsTer7
ENST00000647425.1:c.270_274del ENSP00000496748.1:p.Leu91GlnfsTer7
ENST00000647504.1:c.183_187del ENSP00000495571.1:p.Leu62GlnfsTer7
ENST00000338785.7:c.297_301del ENSP00000342690.3:p.Leu100GlnfsTer7
ENST00000339659.8:c.270_274del ENSP00000340373.3:p.Leu91GlnfsTer7
ENST00000398956.2:c.297_301del ENSP00000381929.2:p.Leu100GlnfsTer7
ENST00000398960.6:c.297_301del ENSP00000381932.2:p.Leu100GlnfsTer7
ENST00000426672.5:c.297_301del ENSP00000412269.1:p.Leu100GlnfsTer7
ENST00000462274.1:n.955_959del
NM_001396.3:c.297_301del NP_001387.2:p.Leu100GlnfsTer7
NM_101395.2:c.297_301del NP_567824.1:p.Leu100GlnfsTer7
NM_130436.2:c.270_274del NP_569120.1:p.Leu91GlnfsTer7
NM_130438.2:c.297_301del NP_569122.1:p.Leu100GlnfsTer7
XM_005260931.3:c.210_214del XP_005260988.1:p.Leu71GlnfsTer7
XM_006723976.2:c.297_301del XP_006724039.1:p.Leu100GlnfsTer7
XM_006723977.2:c.297_301del XP_006724040.1:p.Leu100GlnfsTer7
XM_006723978.2:c.297_301del XP_006724041.1:p.Leu100GlnfsTer7
XM_006723979.2:c.270_274del XP_006724042.1:p.Leu91GlnfsTer7
XM_011529482.1:c.318_322del XP_011527784.1:p.Leu107GlnfsTer7
XM_011529483.1:c.297_301del XP_011527785.1:p.Leu100GlnfsTer7
XM_011529484.1:c.291_295del XP_011527786.1:p.Leu98GlnfsTer7
XM_011529485.1:c.183_187del XP_011527787.1:p.Leu62GlnfsTer7
NM_001347721.1:c.270_274del NP_001334650.1:p.Leu91GlnfsTer7
NM_001347722.1:c.270_274del NP_001334651.1:p.Leu91GlnfsTer7
NM_001347723.1:c.183_187del NP_001334652.1:p.Leu62GlnfsTer7
NM_001396.4:c.297_301del NP_001387.2:p.Leu100GlnfsTer7
XM_006723976.3:c.297_301del XP_006724039.1:p.Leu100GlnfsTer7
XM_006723977.3:c.297_301del XP_006724040.1:p.Leu100GlnfsTer7
XM_006723978.3:c.297_301del XP_006724041.1:p.Leu100GlnfsTer7
XM_011529483.2:c.297_301del XP_011527785.1:p.Leu100GlnfsTer7
XM_017028284.1:c.270_274del XP_016883773.1:p.Leu91GlnfsTer7
XM_017028286.2:c.210_214del XP_016883775.1:p.Leu71GlnfsTer7
XM_024452057.1:c.183_187del XP_024307825.1:p.Leu62GlnfsTer7
NM_001347721.2:c.270_274del MANE Select NP_001334650.1:p.Leu91GlnfsTer7
NM_001347722.2:c.270_274del NP_001334651.1:p.Leu91GlnfsTer7
NM_001347723.2:c.183_187del NP_001334652.1:p.Leu62GlnfsTer7
NM_001396.5:c.297_301del NP_001387.2:p.Leu100GlnfsTer7