Canonical Allele Identifier: CA2654480562

Gene: DYRK1A

Linked Data

• gnomAD v4: 21-37486295-G-GAT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.37486302_37486303dup , CM000683.2:g.37486302_37486303dup	GRCh38
NC_000021.8:g.38858604_38858605dup , CM000683.1:g.38858604_38858605dup	GRCh37
NC_000021.7:g.37780474_37780475dup	NCBI36
NG_009366.1:g.123746_123747dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338785.8:c.517-165_517-164dup	ENSP00000342690.3:n.517-165_517-164dup
ENST00000398960.7:c.517-165_517-164dup	ENSP00000381932.2:n.517-165_517-164dup
ENST00000426672.6:c.517-165_517-164dup	ENSP00000412269.2:n.517-165_517-164dup
ENST00000642309.1:c.403-165_403-164dup	ENSP00000495596.1:n.403-165_403-164dup
ENST00000643355.1:n.206-165_206-164dup
ENST00000643624.1:c.490-165_490-164dup	ENSP00000493627.1:n.490-165_490-164dup
ENST00000643808.1:n.155_156dup
ENST00000643854.1:c.403-165_403-164dup	ENSP00000493653.1:n.403-165_403-164dup
ENST00000644942.1:c.517-165_517-164dup	ENSP00000494544.1:n.517-165_517-164dup
ENST00000645424.1:c.517-165_517-164dup	ENSP00000494897.1:n.517-165_517-164dup
ENST00000645774.1:c.538-165_538-164dup	ENSP00000494536.1:n.538-165_538-164dup
ENST00000646523.1:c.517-165_517-164dup	ENSP00000495632.1:n.517-165_517-164dup
ENST00000646548.1:c.490-165_490-164dup	ENSP00000495908.1:n.490-165_490-164dup
ENST00000647188.2:c.490-165_490-164dup MANE Select	ENSP00000494572.1:n.490-165_490-164dup
ENST00000647425.1:c.490-165_490-164dup	ENSP00000496748.1:n.490-165_490-164dup
ENST00000647504.1:c.403-165_403-164dup	ENSP00000495571.1:n.403-165_403-164dup
ENST00000338785.7:c.517-165_517-164dup	ENSP00000342690.3:n.517-165_517-164dup
ENST00000339659.8:c.490-165_490-164dup	ENSP00000340373.3:n.490-165_490-164dup
ENST00000398956.2:c.517-165_517-164dup	ENSP00000381929.2:n.517-165_517-164dup
ENST00000398960.6:c.517-165_517-164dup	ENSP00000381932.2:n.517-165_517-164dup
ENST00000462274.1:n.1175-165_1175-164dup
NM_001396.3:c.517-165_517-164dup	NP_001387.2:n.517-165_517-164dup
NM_101395.2:c.517-165_517-164dup	NP_567824.1:n.517-165_517-164dup
NM_130436.2:c.490-165_490-164dup	NP_569120.1:n.490-165_490-164dup
NM_130438.2:c.517-165_517-164dup	NP_569122.1:n.517-165_517-164dup
XM_005260931.3:c.430-165_430-164dup	XP_005260988.1:n.430-165_430-164dup
XM_006723976.2:c.517-165_517-164dup	XP_006724039.1:n.517-165_517-164dup
XM_006723977.2:c.517-165_517-164dup	XP_006724040.1:n.517-165_517-164dup
XM_006723978.2:c.517-165_517-164dup	XP_006724041.1:n.517-165_517-164dup
XM_006723979.2:c.490-165_490-164dup	XP_006724042.1:n.490-165_490-164dup
XM_011529482.1:c.538-165_538-164dup	XP_011527784.1:n.538-165_538-164dup
XM_011529483.1:c.517-165_517-164dup	XP_011527785.1:n.517-165_517-164dup
XM_011529484.1:c.511-165_511-164dup	XP_011527786.1:n.511-165_511-164dup
XM_011529485.1:c.403-165_403-164dup	XP_011527787.1:n.403-165_403-164dup
XR_937703.1:n.706+942_706+943dup
XR_937704.1:n.617+3255_617+3256dup
NM_001347721.1:c.490-165_490-164dup	NP_001334650.1:n.490-165_490-164dup
NM_001347722.1:c.490-165_490-164dup	NP_001334651.1:n.490-165_490-164dup
NM_001347723.1:c.403-165_403-164dup	NP_001334652.1:n.403-165_403-164dup
NM_001396.4:c.517-165_517-164dup	NP_001387.2:n.517-165_517-164dup
XM_006723976.3:c.517-165_517-164dup	XP_006724039.1:n.517-165_517-164dup
XM_006723977.3:c.517-165_517-164dup	XP_006724040.1:n.517-165_517-164dup
XM_006723978.3:c.517-165_517-164dup	XP_006724041.1:n.517-165_517-164dup
XM_011529483.2:c.517-165_517-164dup	XP_011527785.1:n.517-165_517-164dup
XM_017028284.1:c.490-165_490-164dup	XP_016883773.1:n.490-165_490-164dup
XM_017028286.2:c.430-165_430-164dup	XP_016883775.1:n.430-165_430-164dup
XM_024452057.1:c.403-165_403-164dup	XP_024307825.1:n.403-165_403-164dup
XR_001755034.1:n.138+3255_138+3256dup
NM_001347721.2:c.490-165_490-164dup MANE Select	NP_001334650.1:n.490-165_490-164dup
NM_001347722.2:c.490-165_490-164dup	NP_001334651.1:n.490-165_490-164dup
NM_001347723.2:c.403-165_403-164dup	NP_001334652.1:n.403-165_403-164dup
NM_001396.5:c.517-165_517-164dup	NP_001387.2:n.517-165_517-164dup