Canonical Allele Identifier: CA9434073

Gene: DYRK1B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39826724C>T , CM000681.2:g.39826724C>T	GRCh38
NC_000019.9:g.40317364C>T , CM000681.1:g.40317364C>T	GRCh37
NC_000019.8:g.45009204C>T	NCBI36
NG_034145.1:g.12510G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004714.3:c.1359G>A MANE Select	NP_004705.1:p.Ala453=
ENST00000323039.10:c.1359G>A MANE Select	ENSP00000312789.4:p.Ala453=
NM_004714.2:c.1359G>A	NP_004705.1:p.Ala453=
NM_006483.2:c.1239G>A	NP_006474.1:p.Ala413=
NM_006483.3:c.1239G>A	NP_006474.1:p.Ala413=
NM_006484.2:c.1275G>A	NP_006475.1:p.Ala425=
NM_006484.3:c.1275G>A	NP_006475.1:p.Ala425=
ENST00000323039.9:c.1359G>A	ENSP00000312789.4:p.Ala453=
ENST00000348817.7:c.1275G>A	ENSP00000221803.4:p.Ala425=
ENST00000430012.6:c.1239G>A	ENSP00000403182.1:p.Ala413=
ENST00000593685.5:c.1359G>A	ENSP00000469863.1:p.Ala453=
ENST00000597639.5:c.1275G>A	ENSP00000472941.1:p.Ala425=
XM_005259395.2:c.1539G>A	XP_005259452.1:p.Ala513=
XM_005259398.3:c.1359G>A	XP_005259455.1:p.Ala453=
XM_005259398.4:c.1359G>A	XP_005259455.1:p.Ala453=
XM_011527469.1:c.1455G>A	XP_011525771.1:p.Ala485=
XM_011527470.1:c.1419G>A	XP_011525772.1:p.Ala473=