Canonical Allele Identifier: CA278530
Gene: DYRK1A HGNC NCBI

Linked Data

ClinVar Variation Id: 204008
dbSNP Id: rs797044523

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.37480762dup , CM000683.2:g.37480762dup GRCh38
NC_000021.8:g.38853064dup , CM000683.1:g.38853064dup GRCh37
NC_000021.7:g.37774934dup NCBI36
NG_009366.1:g.118206dup

Transcript Alleles

HGVS Amino-acid change
ENST00000338785.8:c.452dup ENSP00000342690.3:p.Asn151LysfsTer12
ENST00000398960.7:c.452dup ENSP00000381932.2:p.Asn151LysfsTer12
ENST00000426672.6:c.452dup ENSP00000412269.2:p.Asn151LysfsTer12
ENST00000462274.2:n.346dup
ENST00000642309.1:c.338dup ENSP00000495596.1:p.Asn113LysfsTer12
ENST00000643355.1:n.141dup
ENST00000643624.1:c.425dup ENSP00000493627.1:p.Asn142LysfsTer12
ENST00000643854.1:c.338dup ENSP00000493653.1:p.Asn113LysfsTer12
ENST00000644942.1:c.452dup ENSP00000494544.1:p.Asn151LysfsTer12
ENST00000645424.1:c.452dup ENSP00000494897.1:p.Asn151LysfsTer12
ENST00000645774.1:c.473dup ENSP00000494536.1:p.Asn158LysfsTer12
ENST00000646523.1:c.452dup ENSP00000495632.1:p.Asn151LysfsTer12
ENST00000646548.1:c.425dup ENSP00000495908.1:p.Asn142LysfsTer12
ENST00000647188.2:c.425dup MANE Select ENSP00000494572.1:p.Asn142LysfsTer12
ENST00000647425.1:c.425dup ENSP00000496748.1:p.Asn142LysfsTer12
ENST00000647504.1:c.338dup ENSP00000495571.1:p.Asn113LysfsTer12
ENST00000338785.7:c.452dup ENSP00000342690.3:p.Asn151LysfsTer12
ENST00000339659.8:c.425dup ENSP00000340373.3:p.Asn142LysfsTer12
ENST00000398956.2:c.452dup ENSP00000381929.2:p.Asn151LysfsTer12
ENST00000398960.6:c.452dup ENSP00000381932.2:p.Asn151LysfsTer12
ENST00000462274.1:n.1110dup
NM_001396.3:c.452dup NP_001387.2:p.Asn151LysfsTer12
NM_101395.2:c.452dup NP_567824.1:p.Asn151LysfsTer12
NM_130436.2:c.425dup NP_569120.1:p.Asn142LysfsTer12
NM_130438.2:c.452dup NP_569122.1:p.Asn151LysfsTer12
XM_005260931.3:c.365dup XP_005260988.1:p.Asn122LysfsTer12
XM_006723976.2:c.452dup XP_006724039.1:p.Asn151LysfsTer12
XM_006723977.2:c.452dup XP_006724040.1:p.Asn151LysfsTer12
XM_006723978.2:c.452dup XP_006724041.1:p.Asn151LysfsTer12
XM_006723979.2:c.425dup XP_006724042.1:p.Asn142LysfsTer12
XM_011529482.1:c.473dup XP_011527784.1:p.Asn158LysfsTer12
XM_011529483.1:c.452dup XP_011527785.1:p.Asn151LysfsTer12
XM_011529484.1:c.446dup XP_011527786.1:p.Asn149LysfsTer12
XM_011529485.1:c.338dup XP_011527787.1:p.Asn113LysfsTer12
XR_937703.1:n.707-1641dup
XR_937704.1:n.618-1641dup
NM_001347721.1:c.425dup NP_001334650.1:p.Asn142LysfsTer12
NM_001347722.1:c.425dup NP_001334651.1:p.Asn142LysfsTer12
NM_001347723.1:c.338dup NP_001334652.1:p.Asn113LysfsTer12
NM_001396.4:c.452dup NP_001387.2:p.Asn151LysfsTer12
XM_006723976.3:c.452dup XP_006724039.1:p.Asn151LysfsTer12
XM_006723977.3:c.452dup XP_006724040.1:p.Asn151LysfsTer12
XM_006723978.3:c.452dup XP_006724041.1:p.Asn151LysfsTer12
XM_011529483.2:c.452dup XP_011527785.1:p.Asn151LysfsTer12
XM_017028284.1:c.425dup XP_016883773.1:p.Asn142LysfsTer12
XM_017028286.2:c.365dup XP_016883775.1:p.Asn122LysfsTer12
XM_024452057.1:c.338dup XP_024307825.1:p.Asn113LysfsTer12
XR_001755034.1:n.139-1641dup
NM_001347721.2:c.425dup MANE Select NP_001334650.1:p.Asn142LysfsTer12
NM_001347722.2:c.425dup NP_001334651.1:p.Asn142LysfsTer12
NM_001347723.2:c.338dup NP_001334652.1:p.Asn113LysfsTer12
NM_001396.5:c.452dup NP_001387.2:p.Asn151LysfsTer12