Canonical Allele Identifier: CA507665225

Gene: DYRK1B

Linked Data

• MyVariant Identifiers: chr19:g.40321024G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39830384G>A , CM000681.2:g.39830384G>A	GRCh38
NC_000019.9:g.40321024G>A , CM000681.1:g.40321024G>A	GRCh37
NC_000019.8:g.45012864G>A	NCBI36
NG_034145.1:g.8850C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000323039.10:c.363C>T MANE Select	ENSP00000312789.4:p.Ser121=
ENST00000323039.9:c.363C>T	ENSP00000312789.4:p.Ser121=
ENST00000348817.7:c.363C>T	ENSP00000221803.4:p.Ser121=
ENST00000430012.6:c.363C>T	ENSP00000403182.1:p.Ser121=
ENST00000593685.5:c.363C>T	ENSP00000469863.1:p.Ser121=
ENST00000597639.5:c.363C>T	ENSP00000472941.1:p.Ser121=
ENST00000600611.5:c.363C>T	ENSP00000471609.1:p.Ser121=
ENST00000601972.1:c.363C>T	ENSP00000472861.1:p.Ser121=
NM_004714.2:c.363C>T	NP_004705.1:p.Ser121=
NM_006483.2:c.363C>T	NP_006474.1:p.Ser121=
NM_006484.2:c.363C>T	NP_006475.1:p.Ser121=
XM_005259395.2:c.543C>T	XP_005259452.1:p.Ser181=
XM_005259398.3:c.363C>T	XP_005259455.1:p.Ser121=
XM_011527469.1:c.543C>T	XP_011525771.1:p.Ser181=
XM_011527470.1:c.543C>T	XP_011525772.1:p.Ser181=
XM_005259398.4:c.363C>T	XP_005259455.1:p.Ser121=
NM_004714.3:c.363C>T MANE Select	NP_004705.1:p.Ser121=
NM_006483.3:c.363C>T	NP_006474.1:p.Ser121=
NM_006484.3:c.363C>T	NP_006475.1:p.Ser121=