Canonical Allele Identifier: CA2566357938

Gene: DYRK1A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.37490476_37490477insTTT , CM000683.2:g.37490476_37490477insTTT	GRCh38
NC_000021.8:g.38862778_38862779insTTT , CM000683.1:g.38862778_38862779insTTT	GRCh37
NC_000021.7:g.37784648_37784649insTTT	NCBI36
NG_009366.1:g.127920_127921insTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000338785.8:c.951+15_951+16insTTT	ENSP00000342690.3:n.951+15_951+16insTTT
ENST00000398960.7:c.951+15_951+16insTTT	ENSP00000381932.2:n.951+15_951+16insTTT
ENST00000642309.1:c.837+15_837+16insTTT	ENSP00000495596.1:n.837+15_837+16insTTT
ENST00000643624.1:c.924+15_924+16insTTT	ENSP00000493627.1:n.924+15_924+16insTTT
ENST00000643808.1:n.754+15_754+16insTTT
ENST00000643854.1:c.837+15_837+16insTTT	ENSP00000493653.1:n.837+15_837+16insTTT
ENST00000644367.1:n.315+15_315+16insTTT
ENST00000644942.1:c.951+15_951+16insTTT	ENSP00000494544.1:n.951+15_951+16insTTT
ENST00000645424.1:c.951+15_951+16insTTT	ENSP00000494897.1:n.951+15_951+16insTTT
ENST00000645774.1:c.972+15_972+16insTTT	ENSP00000494536.1:n.972+15_972+16insTTT
ENST00000646224.1:n.366+15_366+16insTTT
ENST00000646523.1:c.951+15_951+16insTTT	ENSP00000495632.1:n.951+15_951+16insTTT
ENST00000646548.1:c.924+15_924+16insTTT	ENSP00000495908.1:n.924+15_924+16insTTT
ENST00000647188.2:c.924+15_924+16insTTT MANE Select	ENSP00000494572.1:n.924+15_924+16insTTT
ENST00000647425.1:c.924+15_924+16insTTT	ENSP00000496748.1:n.924+15_924+16insTTT
ENST00000647504.1:c.837+15_837+16insTTT	ENSP00000495571.1:n.837+15_837+16insTTT
ENST00000338785.7:c.951+15_951+16insTTT	ENSP00000342690.3:n.951+15_951+16insTTT
ENST00000339659.8:c.924+15_924+16insTTT	ENSP00000340373.3:n.924+15_924+16insTTT
ENST00000398956.2:c.951+15_951+16insTTT	ENSP00000381929.2:n.951+15_951+16insTTT
ENST00000398960.6:c.951+15_951+16insTTT	ENSP00000381932.2:n.951+15_951+16insTTT
NM_001396.3:c.951+15_951+16insTTT	NP_001387.2:n.951+15_951+16insTTT
NM_101395.2:c.951+15_951+16insTTT	NP_567824.1:n.951+15_951+16insTTT
NM_130436.2:c.924+15_924+16insTTT	NP_569120.1:n.924+15_924+16insTTT
NM_130438.2:c.951+15_951+16insTTT	NP_569122.1:n.951+15_951+16insTTT
XM_005260931.3:c.864+15_864+16insTTT	XP_005260988.1:n.864+15_864+16insTTT
XM_005260933.3:c.267+15_267+16insTTT	XP_005260990.1:n.267+15_267+16insTTT
XM_006723976.2:c.951+15_951+16insTTT	XP_006724039.1:n.951+15_951+16insTTT
XM_006723977.2:c.951+15_951+16insTTT	XP_006724040.1:n.951+15_951+16insTTT
XM_006723978.2:c.951+15_951+16insTTT	XP_006724041.1:n.951+15_951+16insTTT
XM_006723979.2:c.924+15_924+16insTTT	XP_006724042.1:n.924+15_924+16insTTT
XM_011529482.1:c.972+15_972+16insTTT	XP_011527784.1:n.972+15_972+16insTTT
XM_011529483.1:c.951+15_951+16insTTT	XP_011527785.1:n.951+15_951+16insTTT
XM_011529484.1:c.945+15_945+16insTTT	XP_011527786.1:n.945+15_945+16insTTT
XM_011529485.1:c.837+15_837+16insTTT	XP_011527787.1:n.837+15_837+16insTTT
NM_001347721.1:c.924+15_924+16insTTT	NP_001334650.1:n.924+15_924+16insTTT
NM_001347722.1:c.924+15_924+16insTTT	NP_001334651.1:n.924+15_924+16insTTT
NM_001347723.1:c.837+15_837+16insTTT	NP_001334652.1:n.837+15_837+16insTTT
NM_001396.4:c.951+15_951+16insTTT	NP_001387.2:n.951+15_951+16insTTT
XM_005260933.5:c.267+15_267+16insTTT	XP_005260990.1:n.267+15_267+16insTTT
XM_006723976.3:c.951+15_951+16insTTT	XP_006724039.1:n.951+15_951+16insTTT
XM_006723977.3:c.951+15_951+16insTTT	XP_006724040.1:n.951+15_951+16insTTT
XM_006723978.3:c.951+15_951+16insTTT	XP_006724041.1:n.951+15_951+16insTTT
XM_011529483.2:c.951+15_951+16insTTT	XP_011527785.1:n.951+15_951+16insTTT
XM_017028284.1:c.924+15_924+16insTTT	XP_016883773.1:n.924+15_924+16insTTT
XM_017028286.2:c.864+15_864+16insTTT	XP_016883775.1:n.864+15_864+16insTTT
XM_024452057.1:c.837+15_837+16insTTT	XP_024307825.1:n.837+15_837+16insTTT
NM_001347721.2:c.924+15_924+16insTTT MANE Select	NP_001334650.1:n.924+15_924+16insTTT
NM_001347722.2:c.924+15_924+16insTTT	NP_001334651.1:n.924+15_924+16insTTT
NM_001347723.2:c.837+15_837+16insTTT	NP_001334652.1:n.837+15_837+16insTTT
NM_001396.5:c.951+15_951+16insTTT	NP_001387.2:n.951+15_951+16insTTT