Canonical Allele Identifier: CA409946229
Gene: DYRK1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1314517
ClinVar RCV Id: RCV001773026
dbSNP Id: rs2148601089

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.37486613A>G , CM000683.2:g.37486613A>G GRCh38
NC_000021.8:g.38858915A>G , CM000683.1:g.38858915A>G GRCh37
NC_000021.7:g.37780785A>G NCBI36
NG_009366.1:g.124057A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338785.8:c.663A>G ENSP00000342690.3:p.Ile221Met
ENST00000398960.7:c.663A>G ENSP00000381932.2:p.Ile221Met
ENST00000642309.1:c.549A>G ENSP00000495596.1:p.Ile183Met
ENST00000643355.1:n.352A>G
ENST00000643624.1:c.636A>G ENSP00000493627.1:p.Ile212Met
ENST00000643808.1:n.466A>G
ENST00000643854.1:c.549A>G ENSP00000493653.1:p.Ile183Met
ENST00000644942.1:c.663A>G ENSP00000494544.1:p.Ile221Met
ENST00000645424.1:c.663A>G ENSP00000494897.1:p.Ile221Met
ENST00000645774.1:c.684A>G ENSP00000494536.1:p.Ile228Met
ENST00000646523.1:c.663A>G ENSP00000495632.1:p.Ile221Met
ENST00000646548.1:c.636A>G ENSP00000495908.1:p.Ile212Met
ENST00000647188.2:c.636A>G MANE Select ENSP00000494572.1:p.Ile212Met
ENST00000647425.1:c.636A>G ENSP00000496748.1:p.Ile212Met
ENST00000647504.1:c.549A>G ENSP00000495571.1:p.Ile183Met
ENST00000338785.7:c.663A>G ENSP00000342690.3:p.Ile221Met
ENST00000339659.8:c.636A>G ENSP00000340373.3:p.Ile212Met
ENST00000398956.2:c.663A>G ENSP00000381929.2:p.Ile221Met
ENST00000398960.6:c.663A>G ENSP00000381932.2:p.Ile221Met
NM_001396.3:c.663A>G NP_001387.2:p.Ile221Met
NM_101395.2:c.663A>G NP_567824.1:p.Ile221Met
NM_130436.2:c.636A>G NP_569120.1:p.Ile212Met
NM_130438.2:c.663A>G NP_569122.1:p.Ile221Met
XM_005260931.3:c.576A>G XP_005260988.1:p.Ile192Met
XM_006723976.2:c.663A>G XP_006724039.1:p.Ile221Met
XM_006723977.2:c.663A>G XP_006724040.1:p.Ile221Met
XM_006723978.2:c.663A>G XP_006724041.1:p.Ile221Met
XM_006723979.2:c.636A>G XP_006724042.1:p.Ile212Met
XM_011529482.1:c.684A>G XP_011527784.1:p.Ile228Met
XM_011529483.1:c.663A>G XP_011527785.1:p.Ile221Met
XM_011529484.1:c.657A>G XP_011527786.1:p.Ile219Met
XM_011529485.1:c.549A>G XP_011527787.1:p.Ile183Met
XR_937703.1:n.706+626T>C
XR_937704.1:n.617+2939T>C
NM_001347721.1:c.636A>G NP_001334650.1:p.Ile212Met
NM_001347722.1:c.636A>G NP_001334651.1:p.Ile212Met
NM_001347723.1:c.549A>G NP_001334652.1:p.Ile183Met
NM_001396.4:c.663A>G NP_001387.2:p.Ile221Met
XM_006723976.3:c.663A>G XP_006724039.1:p.Ile221Met
XM_006723977.3:c.663A>G XP_006724040.1:p.Ile221Met
XM_006723978.3:c.663A>G XP_006724041.1:p.Ile221Met
XM_011529483.2:c.663A>G XP_011527785.1:p.Ile221Met
XM_017028284.1:c.636A>G XP_016883773.1:p.Ile212Met
XM_017028286.2:c.576A>G XP_016883775.1:p.Ile192Met
XM_024452057.1:c.549A>G XP_024307825.1:p.Ile183Met
XR_001755034.1:n.138+2939T>C
NM_001347721.2:c.636A>G MANE Select NP_001334650.1:p.Ile212Met
NM_001347722.2:c.636A>G NP_001334651.1:p.Ile212Met
NM_001347723.2:c.549A>G NP_001334652.1:p.Ile183Met
NM_001396.5:c.663A>G NP_001387.2:p.Ile221Met