Canonical Allele Identifier: CA2511177018

Gene: DYRK1A

Linked Data

• gnomAD v4: 21-37492943-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.37492943G>T , CM000683.2:g.37492943G>T	GRCh38
NC_000021.8:g.38865245G>T , CM000683.1:g.38865245G>T	GRCh37
NC_000021.7:g.37787115G>T	NCBI36
NG_009366.1:g.130387G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000338785.8:c.952-74G>T	ENSP00000342690.3:n.952-74G>T
ENST00000398960.7:c.952-74G>T	ENSP00000381932.2:n.952-74G>T
ENST00000642309.1:c.838-74G>T	ENSP00000495596.1:n.838-74G>T
ENST00000643624.1:c.925-74G>T	ENSP00000493627.1:n.925-74G>T
ENST00000643808.1:n.755-74G>T
ENST00000643854.1:c.838-74G>T	ENSP00000493653.1:n.838-74G>T
ENST00000644367.1:n.316-74G>T
ENST00000644942.1:c.952-74G>T	ENSP00000494544.1:n.952-74G>T
ENST00000645424.1:c.952-74G>T	ENSP00000494897.1:n.952-74G>T
ENST00000645774.1:c.973-74G>T	ENSP00000494536.1:n.973-74G>T
ENST00000646224.1:n.367-74G>T
ENST00000646523.1:c.952-74G>T	ENSP00000495632.1:n.952-74G>T
ENST00000646548.1:c.925-74G>T	ENSP00000495908.1:n.925-74G>T
ENST00000647188.2:c.925-74G>T MANE Select	ENSP00000494572.1:n.925-74G>T
ENST00000647425.1:c.925-74G>T	ENSP00000496748.1:n.925-74G>T
ENST00000647504.1:c.838-74G>T	ENSP00000495571.1:n.838-74G>T
ENST00000338785.7:c.952-74G>T	ENSP00000342690.3:n.952-74G>T
ENST00000339659.8:c.925-74G>T	ENSP00000340373.3:n.925-74G>T
ENST00000398956.2:c.952-74G>T	ENSP00000381929.2:n.952-74G>T
ENST00000398960.6:c.952-74G>T	ENSP00000381932.2:n.952-74G>T
NM_001396.3:c.952-74G>T	NP_001387.2:n.952-74G>T
NM_101395.2:c.952-74G>T	NP_567824.1:n.952-74G>T
NM_130436.2:c.925-74G>T	NP_569120.1:n.925-74G>T
NM_130438.2:c.952-74G>T	NP_569122.1:n.952-74G>T
XM_005260931.3:c.865-74G>T	XP_005260988.1:n.865-74G>T
XM_005260933.3:c.268-74G>T	XP_005260990.1:n.268-74G>T
XM_006723976.2:c.952-74G>T	XP_006724039.1:n.952-74G>T
XM_006723977.2:c.952-74G>T	XP_006724040.1:n.952-74G>T
XM_006723978.2:c.952-74G>T	XP_006724041.1:n.952-74G>T
XM_006723979.2:c.925-74G>T	XP_006724042.1:n.925-74G>T
XM_011529482.1:c.973-74G>T	XP_011527784.1:n.973-74G>T
XM_011529483.1:c.952-74G>T	XP_011527785.1:n.952-74G>T
XM_011529484.1:c.946-74G>T	XP_011527786.1:n.946-74G>T
XM_011529485.1:c.838-74G>T	XP_011527787.1:n.838-74G>T
NM_001347721.1:c.925-74G>T	NP_001334650.1:n.925-74G>T
NM_001347722.1:c.925-74G>T	NP_001334651.1:n.925-74G>T
NM_001347723.1:c.838-74G>T	NP_001334652.1:n.838-74G>T
NM_001396.4:c.952-74G>T	NP_001387.2:n.952-74G>T
XM_005260933.5:c.268-74G>T	XP_005260990.1:n.268-74G>T
XM_006723976.3:c.952-74G>T	XP_006724039.1:n.952-74G>T
XM_006723977.3:c.952-74G>T	XP_006724040.1:n.952-74G>T
XM_006723978.3:c.952-74G>T	XP_006724041.1:n.952-74G>T
XM_011529483.2:c.952-74G>T	XP_011527785.1:n.952-74G>T
XM_017028284.1:c.925-74G>T	XP_016883773.1:n.925-74G>T
XM_017028286.2:c.865-74G>T	XP_016883775.1:n.865-74G>T
XM_024452057.1:c.838-74G>T	XP_024307825.1:n.838-74G>T
NM_001347721.2:c.925-74G>T MANE Select	NP_001334650.1:n.925-74G>T
NM_001347722.2:c.925-74G>T	NP_001334651.1:n.925-74G>T
NM_001347723.2:c.838-74G>T	NP_001334652.1:n.838-74G>T
NM_001396.5:c.952-74G>T	NP_001387.2:n.952-74G>T