Canonical Allele Identifier: CA278541
Gene: DYRK1A HGNC NCBI

Linked Data

ClinVar Variation Id: 210898
ClinVar RCV Id: RCV000192601
dbSNP Id: rs797045540
MyVariant Identifiers: chr21:g.38862734T>G (hg19) chr21:g.37490432T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.37490432T>G , CM000683.2:g.37490432T>G GRCh38
NC_000021.8:g.38862734T>G , CM000683.1:g.38862734T>G GRCh37
NC_000021.7:g.37784604T>G NCBI36
NG_009366.1:g.127876T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000338785.8:c.922T>G ENSP00000342690.3:p.Phe308Val
ENST00000398960.7:c.922T>G ENSP00000381932.2:p.Phe308Val
ENST00000642309.1:c.808T>G ENSP00000495596.1:p.Phe270Val
ENST00000643624.1:c.895T>G ENSP00000493627.1:p.Phe299Val
ENST00000643808.1:n.725T>G
ENST00000643854.1:c.808T>G ENSP00000493653.1:p.Phe270Val
ENST00000644367.1:n.286T>G
ENST00000644942.1:c.922T>G ENSP00000494544.1:p.Phe308Val
ENST00000645424.1:c.922T>G ENSP00000494897.1:p.Phe308Val
ENST00000645774.1:c.943T>G ENSP00000494536.1:p.Phe315Val
ENST00000646224.1:n.337T>G
ENST00000646523.1:c.922T>G ENSP00000495632.1:p.Phe308Val
ENST00000646548.1:c.895T>G ENSP00000495908.1:p.Phe299Val
ENST00000647188.2:c.895T>G MANE Select ENSP00000494572.1:p.Phe299Val
ENST00000647425.1:c.895T>G ENSP00000496748.1:p.Phe299Val
ENST00000647504.1:c.808T>G ENSP00000495571.1:p.Phe270Val
ENST00000338785.7:c.922T>G ENSP00000342690.3:p.Phe308Val
ENST00000339659.8:c.895T>G ENSP00000340373.3:p.Phe299Val
ENST00000398956.2:c.922T>G ENSP00000381929.2:p.Phe308Val
ENST00000398960.6:c.922T>G ENSP00000381932.2:p.Phe308Val
NM_001396.3:c.922T>G NP_001387.2:p.Phe308Val
NM_101395.2:c.922T>G NP_567824.1:p.Phe308Val
NM_130436.2:c.895T>G NP_569120.1:p.Phe299Val
NM_130438.2:c.922T>G NP_569122.1:p.Phe308Val
XM_005260931.3:c.835T>G XP_005260988.1:p.Phe279Val
XM_005260933.3:c.238T>G XP_005260990.1:p.Phe80Val
XM_006723976.2:c.922T>G XP_006724039.1:p.Phe308Val
XM_006723977.2:c.922T>G XP_006724040.1:p.Phe308Val
XM_006723978.2:c.922T>G XP_006724041.1:p.Phe308Val
XM_006723979.2:c.895T>G XP_006724042.1:p.Phe299Val
XM_011529482.1:c.943T>G XP_011527784.1:p.Phe315Val
XM_011529483.1:c.922T>G XP_011527785.1:p.Phe308Val
XM_011529484.1:c.916T>G XP_011527786.1:p.Phe306Val
XM_011529485.1:c.808T>G XP_011527787.1:p.Phe270Val
NM_001347721.1:c.895T>G NP_001334650.1:p.Phe299Val
NM_001347722.1:c.895T>G NP_001334651.1:p.Phe299Val
NM_001347723.1:c.808T>G NP_001334652.1:p.Phe270Val
NM_001396.4:c.922T>G NP_001387.2:p.Phe308Val
XM_005260933.5:c.238T>G XP_005260990.1:p.Phe80Val
XM_006723976.3:c.922T>G XP_006724039.1:p.Phe308Val
XM_006723977.3:c.922T>G XP_006724040.1:p.Phe308Val
XM_006723978.3:c.922T>G XP_006724041.1:p.Phe308Val
XM_011529483.2:c.922T>G XP_011527785.1:p.Phe308Val
XM_017028284.1:c.895T>G XP_016883773.1:p.Phe299Val
XM_017028286.2:c.835T>G XP_016883775.1:p.Phe279Val
XM_024452057.1:c.808T>G XP_024307825.1:p.Phe270Val
NM_001347721.2:c.895T>G MANE Select NP_001334650.1:p.Phe299Val
NM_001347722.2:c.895T>G NP_001334651.1:p.Phe299Val
NM_001347723.2:c.808T>G NP_001334652.1:p.Phe270Val
NM_001396.5:c.922T>G NP_001387.2:p.Phe308Val
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