Canonical Allele Identifier: CA403988272

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464802A>T (hg19) ; chr19:g.10354126A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354126A>T , CM000681.2:g.10354126A>T	GRCh38
NC_000019.9:g.10464802A>T , CM000681.1:g.10464802A>T	GRCh37
NC_000019.8:g.10325802A>T	NCBI36
NG_007872.1:g.31447T>A , LRG_121:g.31447T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1173T>A	ENSP00000514307.1:n.*1173T>A
ENST00000525976.6:c.2824T>A	ENSP00000434831.2:p.Ser942Thr
ENST00000527481.3:c.2824T>A	ENSP00000466340.2:p.Ser942Thr
ENST00000529370.6:n.4200T>A
ENST00000529739.2:n.3238T>A
ENST00000530829.2:c.*2375T>A	ENSP00000436826.2:n.*2375T>A
ENST00000531836.6:c.2824T>A	ENSP00000436175.2:p.Ser942Thr
ENST00000533334.2:c.*866T>A	ENSP00000432320.2:n.*866T>A
ENST00000534228.2:n.4283T>A
ENST00000699354.1:n.926T>A
ENST00000699355.1:c.*1929T>A	ENSP00000514328.1:n.*1929T>A
ENST00000699356.1:n.3238T>A
ENST00000699357.1:n.4283T>A
ENST00000699358.1:c.2824T>A	ENSP00000514329.1:p.Ser942Thr
ENST00000699359.1:c.30T>A
ENST00000699360.1:c.2824T>A	ENSP00000514331.1:p.Ser942Thr
ENST00000699368.1:c.28T>A	ENSP00000514335.1:p.Ser10Thr
ENST00000525621.6:c.2824T>A MANE Select	ENSP00000431885.1:p.Ser942Thr
ENST00000264818.10:c.2824T>A	ENSP00000264818.6:p.Ser942Thr
ENST00000524462.5:c.2269T>A	ENSP00000433203.1:p.Ser757Thr
ENST00000525621.5:c.2824T>A	ENSP00000431885.1:p.Ser942Thr
ENST00000527481.2:c.120T>A
ENST00000529412.1:n.496T>A
ENST00000530560.5:c.253T>A	ENSP00000465291.1:p.Ser85Thr
NM_003331.4:c.2824T>A , LRG_121t1:c.2824T>A	NP_003322.3:p.Ser942Thr
XM_011528245.1:c.2824T>A	XP_011526547.1:p.Ser942Thr
XM_011528246.1:c.2527T>A	XP_011526548.1:p.Ser843Thr
XM_011528247.1:c.2527T>A	XP_011526549.1:p.Ser843Thr
XM_011528248.1:c.2824T>A	XP_011526550.1:p.Ser942Thr
XM_011528249.1:c.1498T>A	XP_011526551.1:p.Ser500Thr
XM_011528251.1:c.1081T>A	XP_011526553.1:p.Ser361Thr
XM_011528246.3:c.2527T>A	XP_011526548.1:p.Ser843Thr
XM_011528249.2:c.1498T>A	XP_011526551.1:p.Ser500Thr
XR_001753750.1:n.2981T>A
XR_001753751.1:n.2981T>A
XR_002958353.1:n.3907T>A
NM_003331.5:c.2824T>A MANE Select	NP_003322.3:p.Ser942Thr
NM_001385197.1:c.2824T>A	NP_001372126.1:p.Ser942Thr
NM_001385198.1:c.2824T>A	NP_001372127.1:p.Ser942Thr
NM_001385199.1:c.2638T>A	NP_001372128.1:p.Ser880Thr
NM_001385200.1:c.2821T>A	NP_001372129.1:p.Ser941Thr
NM_001385201.1:c.2626T>A	NP_001372130.1:p.Ser876Thr
NM_001385202.1:c.2740T>A	NP_001372131.1:p.Ser914Thr
NM_001385203.1:c.2905T>A	NP_001372132.1:p.Ser969Thr
NM_001385204.1:c.3034T>A	NP_001372133.1:p.Ser1012Thr
NM_001385205.1:c.2734T>A	NP_001372134.1:p.Ser912Thr
NM_001385206.1:c.2698T>A	NP_001372135.1:p.Ser900Thr
NM_001385207.1:c.2806T>A	NP_001372136.1:p.Ser936Thr