Canonical Allele Identifier: CA403987861

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464759T>G (hg19) ; chr19:g.10354083T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354083T>G , CM000681.2:g.10354083T>G	GRCh38
NC_000019.9:g.10464759T>G , CM000681.1:g.10464759T>G	GRCh37
NC_000019.8:g.10325759T>G	NCBI36
NG_007872.1:g.31490A>C , LRG_121:g.31490A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1216A>C	ENSP00000514307.1:n.*1216A>C
ENST00000525976.6:c.2867A>C	ENSP00000434831.2:p.His956Pro
ENST00000527481.3:c.2867A>C	ENSP00000466340.2:p.His956Pro
ENST00000529370.6:n.4243A>C
ENST00000529739.2:n.3281A>C
ENST00000530829.2:c.*2418A>C	ENSP00000436826.2:n.*2418A>C
ENST00000531836.6:c.2867A>C	ENSP00000436175.2:p.His956Pro
ENST00000533334.2:c.*909A>C	ENSP00000432320.2:n.*909A>C
ENST00000534228.2:n.4326A>C
ENST00000699354.1:n.969A>C
ENST00000699355.1:c.*1972A>C	ENSP00000514328.1:n.*1972A>C
ENST00000699356.1:n.3281A>C
ENST00000699357.1:n.4326A>C
ENST00000699358.1:c.2867A>C	ENSP00000514329.1:p.His956Pro
ENST00000699359.1:c.73A>C
ENST00000699360.1:c.2867A>C	ENSP00000514331.1:p.His956Pro
ENST00000699368.1:c.71A>C	ENSP00000514335.1:p.His24Pro
ENST00000525621.6:c.2867A>C MANE Select	ENSP00000431885.1:p.His956Pro
ENST00000264818.10:c.2867A>C	ENSP00000264818.6:p.His956Pro
ENST00000524462.5:c.2312A>C	ENSP00000433203.1:p.His771Pro
ENST00000525621.5:c.2867A>C	ENSP00000431885.1:p.His956Pro
ENST00000527481.2:c.163A>C
ENST00000529412.1:n.539A>C
ENST00000530560.5:c.296A>C	ENSP00000465291.1:p.His99Pro
ENST00000592137.1:n.21A>C
NM_003331.4:c.2867A>C , LRG_121t1:c.2867A>C	NP_003322.3:p.His956Pro
XM_011528245.1:c.2867A>C	XP_011526547.1:p.His956Pro
XM_011528246.1:c.2570A>C	XP_011526548.1:p.His857Pro
XM_011528247.1:c.2570A>C	XP_011526549.1:p.His857Pro
XM_011528248.1:c.2867A>C	XP_011526550.1:p.His956Pro
XM_011528249.1:c.1541A>C	XP_011526551.1:p.His514Pro
XM_011528251.1:c.1124A>C	XP_011526553.1:p.His375Pro
XM_011528246.3:c.2570A>C	XP_011526548.1:p.His857Pro
XM_011528249.2:c.1541A>C	XP_011526551.1:p.His514Pro
XR_001753750.1:n.3024A>C
XR_001753751.1:n.3024A>C
XR_002958353.1:n.3950A>C
NM_003331.5:c.2867A>C MANE Select	NP_003322.3:p.His956Pro
NM_001385197.1:c.2867A>C	NP_001372126.1:p.His956Pro
NM_001385198.1:c.2867A>C	NP_001372127.1:p.His956Pro
NM_001385199.1:c.2681A>C	NP_001372128.1:p.His894Pro
NM_001385200.1:c.2864A>C	NP_001372129.1:p.His955Pro
NM_001385201.1:c.2669A>C	NP_001372130.1:p.His890Pro
NM_001385202.1:c.2783A>C	NP_001372131.1:p.His928Pro
NM_001385203.1:c.2948A>C	NP_001372132.1:p.His983Pro
NM_001385204.1:c.3077A>C	NP_001372133.1:p.His1026Pro
NM_001385205.1:c.2777A>C	NP_001372134.1:p.His926Pro
NM_001385206.1:c.2741A>C	NP_001372135.1:p.His914Pro
NM_001385207.1:c.2849A>C	NP_001372136.1:p.His950Pro