Canonical Allele Identifier: CA2388476115

Gene: DYRK1A

Linked Data

• dbSNP Id: rs1137600

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.37450958A>T , CM000683.2:g.37450958A>T	GRCh38
NC_000021.8:g.38823260A>T , CM000683.1:g.38823260A>T	GRCh37
NC_000021.7:g.37745130A>T	NCBI36
NG_009366.1:g.88402A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000338785.8:c.11-21726A>T	ENSP00000342690.3:n.11-21726A>T
ENST00000398960.7:c.11-21726A>T	ENSP00000381932.2:n.11-21726A>T
ENST00000426672.6:c.11-21726A>T	ENSP00000412269.2:n.11-21726A>T
ENST00000455097.6:c.-78+20558A>T	ENSP00000398483.2:n.-78+20558A>T
ENST00000642309.1:c.-78+20558A>T	ENSP00000495596.1:n.-78+20558A>T
ENST00000643551.1:c.11-21726A>T	ENSP00000494698.1:n.11-21726A>T
ENST00000643624.1:c.11-21726A>T	ENSP00000493627.1:n.11-21726A>T
ENST00000643854.1:c.-77-21726A>T	ENSP00000493653.1:n.-77-21726A>T
ENST00000644942.1:c.11-21726A>T	ENSP00000494544.1:n.11-21726A>T
ENST00000645424.1:c.11-21726A>T	ENSP00000494897.1:n.11-21726A>T
ENST00000645774.1:c.-148-5172A>T	ENSP00000494536.1:n.-148-5172A>T
ENST00000646523.1:c.11-21726A>T	ENSP00000495632.1:n.11-21726A>T
ENST00000646548.1:c.11-21726A>T	ENSP00000495908.1:n.11-21726A>T
ENST00000647188.2:c.11-21726A>T MANE Select	ENSP00000494572.1:n.11-21726A>T
ENST00000647425.1:c.11-21726A>T	ENSP00000496748.1:n.11-21726A>T
ENST00000647504.1:c.-77-21726A>T	ENSP00000495571.1:n.-77-21726A>T
ENST00000338785.7:c.11-21726A>T	ENSP00000342690.3:n.11-21726A>T
ENST00000339659.8:c.11-21726A>T	ENSP00000340373.3:n.11-21726A>T
ENST00000398956.2:c.11-21726A>T	ENSP00000381929.2:n.11-21726A>T
ENST00000398960.6:c.11-21726A>T	ENSP00000381932.2:n.11-21726A>T
ENST00000426672.5:c.11-21726A>T	ENSP00000412269.1:n.11-21726A>T
ENST00000455097.5:c.11-21726A>T	ENSP00000398483.1:n.11-21726A>T
ENST00000462274.1:n.696-21726A>T
ENST00000498351.1:n.192+20558A>T
NM_001396.3:c.11-21726A>T	NP_001387.2:n.11-21726A>T
NM_101395.2:c.11-21726A>T	NP_567824.1:n.11-21726A>T
NM_130436.2:c.11-21726A>T	NP_569120.1:n.11-21726A>T
NM_130438.2:c.11-21726A>T	NP_569122.1:n.11-21726A>T
XM_005260931.3:c.-78+20558A>T	XP_005260988.1:n.-78+20558A>T
XM_006723976.2:c.11-21726A>T	XP_006724039.1:n.11-21726A>T
XM_006723977.2:c.11-21726A>T	XP_006724040.1:n.11-21726A>T
XM_006723978.2:c.11-21726A>T	XP_006724041.1:n.11-21726A>T
XM_006723979.2:c.11-21726A>T	XP_006724042.1:n.11-21726A>T
XM_011529483.1:c.11-21726A>T	XP_011527785.1:n.11-21726A>T
XM_011529485.1:c.-77-21726A>T	XP_011527787.1:n.-77-21726A>T
NM_001347721.1:c.11-21726A>T	NP_001334650.1:n.11-21726A>T
NM_001347722.1:c.11-21726A>T	NP_001334651.1:n.11-21726A>T
NM_001347723.1:c.-77-21726A>T	NP_001334652.1:n.-77-21726A>T
NM_001396.4:c.11-21726A>T	NP_001387.2:n.11-21726A>T
XM_006723976.3:c.11-21726A>T	XP_006724039.1:n.11-21726A>T
XM_006723977.3:c.11-21726A>T	XP_006724040.1:n.11-21726A>T
XM_006723978.3:c.11-21726A>T	XP_006724041.1:n.11-21726A>T
XM_011529483.2:c.11-21726A>T	XP_011527785.1:n.11-21726A>T
XM_017028284.1:c.11-21726A>T	XP_016883773.1:n.11-21726A>T
XM_017028286.2:c.-78+20558A>T	XP_016883775.1:n.-78+20558A>T
XM_024452057.1:c.-78+20558A>T	XP_024307825.1:n.-78+20558A>T
NM_001347721.2:c.11-21726A>T MANE Select	NP_001334650.1:n.11-21726A>T
NM_001347722.2:c.11-21726A>T	NP_001334651.1:n.11-21726A>T
NM_001347723.2:c.-77-21726A>T	NP_001334652.1:n.-77-21726A>T
NM_001396.5:c.11-21726A>T	NP_001387.2:n.11-21726A>T