Canonical Allele Identifier: CA10024162

Gene: DYRK1A

Linked Data

• ClinVar Variation Id: 864077
• ClinVar RCV Id: RCV001071180
• dbSNP Id: rs756765804
• ExAC: 21:38884656 A / T
• gnomAD v2: 21-38884656-A-T
• gnomAD v4: 21-37512353-A-T
• MyVariant Identifiers: chr21:g.38884656A>T (hg19) ; chr21:g.37512353A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.37512353A>T , CM000683.2:g.37512353A>T	GRCh38
NC_000021.8:g.38884656A>T , CM000683.1:g.38884656A>T	GRCh37
NC_000021.7:g.37806526A>T	NCBI36
NG_009366.1:g.149798A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000338785.8:c.*490A>T	ENSP00000342690.3:n.*490A>T
ENST00000398960.7:c.2114A>T	ENSP00000381932.2:p.Tyr705Phe
ENST00000643624.1:c.2087A>T	ENSP00000493627.1:p.Tyr696Phe
ENST00000644942.1:c.2114A>T	ENSP00000494544.1:p.Tyr705Phe
ENST00000646224.1:n.1529A>T
ENST00000646548.1:c.2087A>T	ENSP00000495908.1:p.Tyr696Phe
ENST00000647188.2:c.2087A>T MANE Select	ENSP00000494572.1:p.Tyr696Phe
ENST00000647425.1:c.2087A>T	ENSP00000496748.1:p.Tyr696Phe
ENST00000647504.1:c.2000A>T	ENSP00000495571.1:p.Tyr667Phe
ENST00000338785.7:c.*490A>T	ENSP00000342690.3:n.*490A>T
ENST00000339659.8:c.2087A>T	ENSP00000340373.3:p.Tyr696Phe
ENST00000398960.6:c.2114A>T	ENSP00000381932.2:p.Tyr705Phe
NM_001396.3:c.2114A>T	NP_001387.2:p.Tyr705Phe
NM_101395.2:c.*490A>T	NP_567824.1:n.*490A>T
NM_130436.2:c.2087A>T	NP_569120.1:p.Tyr696Phe
NM_130438.2:c.*399A>T	NP_569122.1:n.*399A>T
XM_005260931.3:c.2027A>T	XP_005260988.1:p.Tyr676Phe
XM_005260933.3:c.1430A>T	XP_005260990.1:p.Tyr477Phe
XM_006723976.2:c.2114A>T	XP_006724039.1:p.Tyr705Phe
XM_006723977.2:c.2114A>T	XP_006724040.1:p.Tyr705Phe
XM_006723978.2:c.2114A>T	XP_006724041.1:p.Tyr705Phe
XM_006723979.2:c.2087A>T	XP_006724042.1:p.Tyr696Phe
XM_011529482.1:c.2135A>T	XP_011527784.1:p.Tyr712Phe
XM_011529483.1:c.2114A>T	XP_011527785.1:p.Tyr705Phe
XM_011529484.1:c.2108A>T	XP_011527786.1:p.Tyr703Phe
XM_011529485.1:c.2000A>T	XP_011527787.1:p.Tyr667Phe
NM_001347721.1:c.2087A>T	NP_001334650.1:p.Tyr696Phe
NM_001347722.1:c.2087A>T	NP_001334651.1:p.Tyr696Phe
NM_001347723.1:c.2000A>T	NP_001334652.1:p.Tyr667Phe
NM_001396.4:c.2114A>T	NP_001387.2:p.Tyr705Phe
XM_005260933.5:c.1430A>T	XP_005260990.1:p.Tyr477Phe
XM_006723976.3:c.2114A>T	XP_006724039.1:p.Tyr705Phe
XM_006723977.3:c.2114A>T	XP_006724040.1:p.Tyr705Phe
XM_006723978.3:c.2114A>T	XP_006724041.1:p.Tyr705Phe
XM_011529483.2:c.2114A>T	XP_011527785.1:p.Tyr705Phe
XM_017028284.1:c.2087A>T	XP_016883773.1:p.Tyr696Phe
XM_017028286.2:c.2027A>T	XP_016883775.1:p.Tyr676Phe
XM_024452057.1:c.2000A>T	XP_024307825.1:p.Tyr667Phe
NM_001347721.2:c.2087A>T MANE Select	NP_001334650.1:p.Tyr696Phe
NM_001347722.2:c.2087A>T	NP_001334651.1:p.Tyr696Phe
NM_001347723.2:c.2000A>T	NP_001334652.1:p.Tyr667Phe
NM_001396.5:c.2114A>T	NP_001387.2:p.Tyr705Phe