Canonical Allele Identifier: CA2335702640
Gene: DYRK1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39830387G= , CM000681.2:g.39830387G= GRCh38
NC_000019.9:g.40321027G= , CM000681.1:g.40321027G= GRCh37
NC_000019.8:g.45012867G= NCBI36
NG_034145.1:g.8847C=

Transcript Alleles

HGVS Amino-acid change
ENST00000323039.10:c.360C= MANE Select ENSP00000312789.4:p.Gly120=
ENST00000323039.9:c.360C= ENSP00000312789.4:p.Gly120=
ENST00000348817.7:c.360C= ENSP00000221803.4:p.Gly120=
ENST00000430012.6:c.360C= ENSP00000403182.1:p.Gly120=
ENST00000593685.5:c.360C= ENSP00000469863.1:p.Gly120=
ENST00000597639.5:c.360C= ENSP00000472941.1:p.Gly120=
ENST00000600611.5:c.360C= ENSP00000471609.1:p.Gly120=
ENST00000601972.1:c.360C= ENSP00000472861.1:p.Gly120=
NM_004714.2:c.360C= NP_004705.1:p.Gly120=
NM_006483.2:c.360C= NP_006474.1:p.Gly120=
NM_006484.2:c.360C= NP_006475.1:p.Gly120=
XM_005259395.2:c.540C= XP_005259452.1:p.Gly180=
XM_005259398.3:c.360C= XP_005259455.1:p.Gly120=
XM_011527469.1:c.540C= XP_011525771.1:p.Gly180=
XM_011527470.1:c.540C= XP_011525772.1:p.Gly180=
XM_005259398.4:c.360C= XP_005259455.1:p.Gly120=
NM_004714.3:c.360C= MANE Select NP_004705.1:p.Gly120=
NM_006483.3:c.360C= NP_006474.1:p.Gly120=
NM_006484.3:c.360C= NP_006475.1:p.Gly120=