Canonical Allele Identifier: CA320448412
Gene: DYRK1A HGNC NCBI

Linked Data

dbSNP Id: rs11701483

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.37427806A>G , CM000683.2:g.37427806A>G GRCh38
NC_000021.8:g.38800108A>G , CM000683.1:g.38800108A>G GRCh37
NC_000021.7:g.37721978A>G NCBI36
NG_009366.1:g.65250A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000338785.8:c.10+7422A>G ENSP00000342690.3:n.10+7422A>G
ENST00000398960.7:c.10+7422A>G ENSP00000381932.2:n.10+7422A>G
ENST00000426672.6:c.10+7422A>G ENSP00000412269.2:n.10+7422A>G
ENST00000455097.6:c.-209-2463A>G ENSP00000398483.2:n.-209-2463A>G
ENST00000642309.1:c.-251-1061A>G ENSP00000495596.1:n.-251-1061A>G
ENST00000643551.1:c.10+7422A>G ENSP00000494698.1:n.10+7422A>G
ENST00000643624.1:c.10+7422A>G ENSP00000493627.1:n.10+7422A>G
ENST00000643854.1:c.-78+5940A>G ENSP00000493653.1:n.-78+5940A>G
ENST00000644942.1:c.10+7422A>G ENSP00000494544.1:n.10+7422A>G
ENST00000645424.1:c.10+7422A>G ENSP00000494897.1:n.10+7422A>G
ENST00000645774.1:c.-149+7422A>G ENSP00000494536.1:n.-149+7422A>G
ENST00000646523.1:c.10+7422A>G ENSP00000495632.1:n.10+7422A>G
ENST00000646548.1:c.10+7422A>G ENSP00000495908.1:n.10+7422A>G
ENST00000647188.2:c.10+7422A>G MANE Select ENSP00000494572.1:n.10+7422A>G
ENST00000647425.1:c.10+7422A>G ENSP00000496748.1:n.10+7422A>G
ENST00000647504.1:c.-77-44878A>G ENSP00000495571.1:n.-77-44878A>G
ENST00000338785.7:c.10+7422A>G ENSP00000342690.3:n.10+7422A>G
ENST00000339659.8:c.10+7422A>G ENSP00000340373.3:n.10+7422A>G
ENST00000398956.2:c.10+7422A>G ENSP00000381929.2:n.10+7422A>G
ENST00000398960.6:c.10+7422A>G ENSP00000381932.2:n.10+7422A>G
ENST00000426672.5:c.10+7422A>G ENSP00000412269.1:n.10+7422A>G
ENST00000455097.5:c.10+7422A>G ENSP00000398483.1:n.10+7422A>G
ENST00000462274.1:n.696-44878A>G
ENST00000498351.1:n.61-2463A>G
NM_001396.3:c.10+7422A>G NP_001387.2:n.10+7422A>G
NM_101395.2:c.10+7422A>G NP_567824.1:n.10+7422A>G
NM_130436.2:c.10+7422A>G NP_569120.1:n.10+7422A>G
NM_130438.2:c.10+7422A>G NP_569122.1:n.10+7422A>G
XM_005260931.3:c.-209-2463A>G XP_005260988.1:n.-209-2463A>G
XM_006723976.2:c.10+7422A>G XP_006724039.1:n.10+7422A>G
XM_006723977.2:c.10+7422A>G XP_006724040.1:n.10+7422A>G
XM_006723978.2:c.10+7422A>G XP_006724041.1:n.10+7422A>G
XM_006723979.2:c.10+7422A>G XP_006724042.1:n.10+7422A>G
XM_011529483.1:c.10+7422A>G XP_011527785.1:n.10+7422A>G
XM_011529485.1:c.-77-44878A>G XP_011527787.1:n.-77-44878A>G
NM_001347721.1:c.10+7422A>G NP_001334650.1:n.10+7422A>G
NM_001347722.1:c.10+7422A>G NP_001334651.1:n.10+7422A>G
NM_001347723.1:c.-77-44878A>G NP_001334652.1:n.-77-44878A>G
NM_001396.4:c.10+7422A>G NP_001387.2:n.10+7422A>G
XM_006723976.3:c.10+7422A>G XP_006724039.1:n.10+7422A>G
XM_006723977.3:c.10+7422A>G XP_006724040.1:n.10+7422A>G
XM_006723978.3:c.10+7422A>G XP_006724041.1:n.10+7422A>G
XM_011529483.2:c.10+7422A>G XP_011527785.1:n.10+7422A>G
XM_017028284.1:c.10+7422A>G XP_016883773.1:n.10+7422A>G
XM_017028286.2:c.-251-1061A>G XP_016883775.1:n.-251-1061A>G
XM_024452057.1:c.-251-1061A>G XP_024307825.1:n.-251-1061A>G
NM_001347721.2:c.10+7422A>G MANE Select NP_001334650.1:n.10+7422A>G
NM_001347722.2:c.10+7422A>G NP_001334651.1:n.10+7422A>G
NM_001347723.2:c.-77-44878A>G NP_001334652.1:n.-77-44878A>G
NM_001396.5:c.10+7422A>G NP_001387.2:n.10+7422A>G