Canonical Allele Identifier: CA405828449

Gene: DYRK1B

Linked Data

• MyVariant Identifiers: chr19:g.40321022A>C (hg19) ; chr19:g.39830382A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39830382A>C , CM000681.2:g.39830382A>C	GRCh38
NC_000019.9:g.40321022A>C , CM000681.1:g.40321022A>C	GRCh37
NC_000019.8:g.45012862A>C	NCBI36
NG_034145.1:g.8852T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323039.10:c.365T>G MANE Select	ENSP00000312789.4:p.Phe122Cys
ENST00000323039.9:c.365T>G	ENSP00000312789.4:p.Phe122Cys
ENST00000348817.7:c.365T>G	ENSP00000221803.4:p.Phe122Cys
ENST00000430012.6:c.365T>G	ENSP00000403182.1:p.Phe122Cys
ENST00000593685.5:c.365T>G	ENSP00000469863.1:p.Phe122Cys
ENST00000597639.5:c.365T>G	ENSP00000472941.1:p.Phe122Cys
ENST00000600611.5:c.365T>G	ENSP00000471609.1:p.Phe122Cys
ENST00000601972.1:c.365T>G	ENSP00000472861.1:p.Phe122Cys
NM_004714.2:c.365T>G	NP_004705.1:p.Phe122Cys
NM_006483.2:c.365T>G	NP_006474.1:p.Phe122Cys
NM_006484.2:c.365T>G	NP_006475.1:p.Phe122Cys
XM_005259395.2:c.545T>G	XP_005259452.1:p.Phe182Cys
XM_005259398.3:c.365T>G	XP_005259455.1:p.Phe122Cys
XM_011527469.1:c.545T>G	XP_011525771.1:p.Phe182Cys
XM_011527470.1:c.545T>G	XP_011525772.1:p.Phe182Cys
XM_005259398.4:c.365T>G	XP_005259455.1:p.Phe122Cys
NM_004714.3:c.365T>G MANE Select	NP_004705.1:p.Phe122Cys
NM_006483.3:c.365T>G	NP_006474.1:p.Phe122Cys
NM_006484.3:c.365T>G	NP_006475.1:p.Phe122Cys