Canonical Allele Identifier: CA403983291

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463198T>G (hg19) ; chr19:g.10352522T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352522T>G , CM000681.2:g.10352522T>G	GRCh38
NC_000019.9:g.10463198T>G , CM000681.1:g.10463198T>G	GRCh37
NC_000019.8:g.10324198T>G	NCBI36
NG_007872.1:g.33051A>C , LRG_121:g.33051A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1579A>C	ENSP00000514307.1:n.*1579A>C
ENST00000525976.6:c.3230A>C	ENSP00000434831.2:p.Lys1077Thr
ENST00000527481.3:c.3111A>C	ENSP00000466340.2:p.Ter1037Tyr
ENST00000529370.6:n.4606A>C
ENST00000529739.2:n.4039A>C
ENST00000530829.2:c.*2781A>C	ENSP00000436826.2:n.*2781A>C
ENST00000531836.6:c.3230A>C	ENSP00000436175.2:p.Lys1077Thr
ENST00000533334.2:c.*1242+404A>C	ENSP00000432320.2:n.*1242+404A>C
ENST00000534228.2:n.5054+404A>C
ENST00000699354.1:n.1332A>C
ENST00000699355.1:c.*2730A>C	ENSP00000514328.1:n.*2730A>C
ENST00000699356.1:n.4039A>C
ENST00000699357.1:n.5084A>C
ENST00000699358.1:c.3200+404A>C	ENSP00000514329.1:n.3200+404A>C
ENST00000699359.1:c.404A>C
ENST00000699360.1:c.3188A>C	ENSP00000514331.1:p.Lys1063Thr
ENST00000699361.1:n.264A>C
ENST00000699362.1:c.126A>C	ENSP00000514332.1:p.Ter42Tyr
ENST00000699363.1:c.126A>C	ENSP00000514333.1:p.Ter42Tyr
ENST00000699364.1:n.230A>C
ENST00000699365.1:c.299A>C	ENSP00000514334.1:p.Lys100Thr
ENST00000699366.1:n.111+1292A>C
ENST00000699367.1:n.111+1292A>C
ENST00000699368.1:c.717A>C	ENSP00000514335.1:n.717A>C
ENST00000525621.6:c.3230A>C MANE Select	ENSP00000431885.1:p.Lys1077Thr
ENST00000264818.10:c.3230A>C	ENSP00000264818.6:p.Lys1077Thr
ENST00000524462.5:c.2675A>C	ENSP00000433203.1:p.Lys892Thr
ENST00000525621.5:c.3230A>C	ENSP00000431885.1:p.Lys1077Thr
ENST00000527481.2:c.407A>C
ENST00000529422.1:n.116+500A>C
ENST00000529739.1:c.299A>C	ENSP00000436155.1:p.Lys100Thr
ENST00000530220.1:n.331+404A>C
ENST00000530560.5:c.337+1520A>C	ENSP00000465291.1:n.337+1520A>C
ENST00000592137.1:n.384A>C
NM_003331.4:c.3230A>C , LRG_121t1:c.3230A>C	NP_003322.3:p.Lys1077Thr
XM_011528245.1:c.3230A>C	XP_011526547.1:p.Lys1077Thr
XM_011528246.1:c.2933A>C	XP_011526548.1:p.Lys978Thr
XM_011528247.1:c.2933A>C	XP_011526549.1:p.Lys978Thr
XM_011528248.1:c.3200+404A>C	XP_011526550.1:n.3200+404A>C
XM_011528249.1:c.1904A>C	XP_011526551.1:p.Lys635Thr
XM_011528251.1:c.1487A>C	XP_011526553.1:p.Lys496Thr
XM_011528246.3:c.2933A>C	XP_011526548.1:p.Lys978Thr
XM_011528249.2:c.1904A>C	XP_011526551.1:p.Lys635Thr
XR_001753750.1:n.3357+404A>C
XR_001753751.1:n.3782A>C
XR_002958353.1:n.4708A>C
NM_003331.5:c.3230A>C MANE Select	NP_003322.3:p.Lys1077Thr
NM_001385197.1:c.3230A>C	NP_001372126.1:p.Lys1077Thr
NM_001385198.1:c.3168+436A>C	NP_001372127.1:n.3168+436A>C
NM_001385199.1:c.3044A>C	NP_001372128.1:p.Lys1015Thr
NM_001385200.1:c.3227A>C	NP_001372129.1:p.Lys1076Thr
NM_001385201.1:c.3032A>C	NP_001372130.1:p.Lys1011Thr
NM_001385202.1:c.3146A>C	NP_001372131.1:p.Lys1049Thr
NM_001385203.1:c.3311A>C	NP_001372132.1:p.Lys1104Thr
NM_001385204.1:c.3440A>C	NP_001372133.1:p.Lys1147Thr
NM_001385205.1:c.3140A>C	NP_001372134.1:p.Lys1047Thr
NM_001385206.1:c.3104A>C	NP_001372135.1:p.Lys1035Thr
NM_001385207.1:c.3212A>C	NP_001372136.1:p.Lys1071Thr