Canonical Allele Identifier: CA403988137

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464792T>G (hg19) ; chr19:g.10354116T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354116T>G , CM000681.2:g.10354116T>G	GRCh38
NC_000019.9:g.10464792T>G , CM000681.1:g.10464792T>G	GRCh37
NC_000019.8:g.10325792T>G	NCBI36
NG_007872.1:g.31457A>C , LRG_121:g.31457A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1183A>C	ENSP00000514307.1:n.*1183A>C
ENST00000525976.6:c.2834A>C	ENSP00000434831.2:p.Lys945Thr
ENST00000527481.3:c.2834A>C	ENSP00000466340.2:p.Lys945Thr
ENST00000529370.6:n.4210A>C
ENST00000529739.2:n.3248A>C
ENST00000530829.2:c.*2385A>C	ENSP00000436826.2:n.*2385A>C
ENST00000531836.6:c.2834A>C	ENSP00000436175.2:p.Lys945Thr
ENST00000533334.2:c.*876A>C	ENSP00000432320.2:n.*876A>C
ENST00000534228.2:n.4293A>C
ENST00000699354.1:n.936A>C
ENST00000699355.1:c.*1939A>C	ENSP00000514328.1:n.*1939A>C
ENST00000699356.1:n.3248A>C
ENST00000699357.1:n.4293A>C
ENST00000699358.1:c.2834A>C	ENSP00000514329.1:p.Lys945Thr
ENST00000699359.1:c.40A>C
ENST00000699360.1:c.2834A>C	ENSP00000514331.1:p.Lys945Thr
ENST00000699368.1:c.38A>C	ENSP00000514335.1:p.Lys13Thr
ENST00000525621.6:c.2834A>C MANE Select	ENSP00000431885.1:p.Lys945Thr
ENST00000264818.10:c.2834A>C	ENSP00000264818.6:p.Lys945Thr
ENST00000524462.5:c.2279A>C	ENSP00000433203.1:p.Lys760Thr
ENST00000525621.5:c.2834A>C	ENSP00000431885.1:p.Lys945Thr
ENST00000527481.2:c.130A>C
ENST00000529412.1:n.506A>C
ENST00000530560.5:c.263A>C	ENSP00000465291.1:p.Lys88Thr
NM_003331.4:c.2834A>C , LRG_121t1:c.2834A>C	NP_003322.3:p.Lys945Thr
XM_011528245.1:c.2834A>C	XP_011526547.1:p.Lys945Thr
XM_011528246.1:c.2537A>C	XP_011526548.1:p.Lys846Thr
XM_011528247.1:c.2537A>C	XP_011526549.1:p.Lys846Thr
XM_011528248.1:c.2834A>C	XP_011526550.1:p.Lys945Thr
XM_011528249.1:c.1508A>C	XP_011526551.1:p.Lys503Thr
XM_011528251.1:c.1091A>C	XP_011526553.1:p.Lys364Thr
XM_011528246.3:c.2537A>C	XP_011526548.1:p.Lys846Thr
XM_011528249.2:c.1508A>C	XP_011526551.1:p.Lys503Thr
XR_001753750.1:n.2991A>C
XR_001753751.1:n.2991A>C
XR_002958353.1:n.3917A>C
NM_003331.5:c.2834A>C MANE Select	NP_003322.3:p.Lys945Thr
NM_001385197.1:c.2834A>C	NP_001372126.1:p.Lys945Thr
NM_001385198.1:c.2834A>C	NP_001372127.1:p.Lys945Thr
NM_001385199.1:c.2648A>C	NP_001372128.1:p.Lys883Thr
NM_001385200.1:c.2831A>C	NP_001372129.1:p.Lys944Thr
NM_001385201.1:c.2636A>C	NP_001372130.1:p.Lys879Thr
NM_001385202.1:c.2750A>C	NP_001372131.1:p.Lys917Thr
NM_001385203.1:c.2915A>C	NP_001372132.1:p.Lys972Thr
NM_001385204.1:c.3044A>C	NP_001372133.1:p.Lys1015Thr
NM_001385205.1:c.2744A>C	NP_001372134.1:p.Lys915Thr
NM_001385206.1:c.2708A>C	NP_001372135.1:p.Lys903Thr
NM_001385207.1:c.2816A>C	NP_001372136.1:p.Lys939Thr