Canonical Allele Identifier: CA403982903

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463121T>A (hg19) ; chr19:g.10352445T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352445T>A , CM000681.2:g.10352445T>A	GRCh38
NC_000019.9:g.10463121T>A , CM000681.1:g.10463121T>A	GRCh37
NC_000019.8:g.10324121T>A	NCBI36
NG_007872.1:g.33128A>T , LRG_121:g.33128A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.*1656A>T	ENSP00000514307.1:n.*1656A>T
ENST00000525976.6:c.3307A>T	ENSP00000434831.2:p.Ser1103Cys
ENST00000527481.3:c.*77A>T	ENSP00000466340.2:n.*77A>T
ENST00000529370.6:n.4683A>T
ENST00000529739.2:n.4116A>T
ENST00000530829.2:c.*2858A>T	ENSP00000436826.2:n.*2858A>T
ENST00000531836.6:c.3307A>T	ENSP00000436175.2:p.Ser1103Cys
ENST00000533334.2:c.*1242+481A>T	ENSP00000432320.2:n.*1242+481A>T
ENST00000534228.2:n.5054+481A>T
ENST00000699354.1:n.1409A>T
ENST00000699355.1:c.*2807A>T	ENSP00000514328.1:n.*2807A>T
ENST00000699356.1:n.4116A>T
ENST00000699357.1:n.5161A>T
ENST00000699358.1:c.3200+481A>T	ENSP00000514329.1:n.3200+481A>T
ENST00000699359.1:c.481A>T
ENST00000699360.1:c.3265A>T	ENSP00000514331.1:p.Ser1089Cys
ENST00000699361.1:n.341A>T
ENST00000699362.1:c.203A>T	ENSP00000514332.1:n.203A>T
ENST00000699363.1:c.203A>T	ENSP00000514333.1:n.203A>T
ENST00000699364.1:n.307A>T
ENST00000699365.1:c.376A>T	ENSP00000514334.1:p.Ser126Cys
ENST00000699366.1:n.111+1369A>T
ENST00000699367.1:n.112-1283A>T
ENST00000699368.1:c.794A>T	ENSP00000514335.1:n.794A>T
ENST00000525621.6:c.3307A>T MANE Select	ENSP00000431885.1:p.Ser1103Cys
ENST00000264818.10:c.3307A>T	ENSP00000264818.6:p.Ser1103Cys
ENST00000524462.5:c.2752A>T	ENSP00000433203.1:p.Ser918Cys
ENST00000525621.5:c.3307A>T	ENSP00000431885.1:p.Ser1103Cys
ENST00000525976.5:c.48A>T
ENST00000527481.2:c.484A>T
ENST00000529422.1:n.116+577A>T
ENST00000529739.1:c.376A>T	ENSP00000436155.1:p.Ser126Cys
ENST00000530220.1:n.331+481A>T
ENST00000530560.5:c.338-1477A>T	ENSP00000465291.1:n.338-1477A>T
ENST00000592137.1:n.461A>T
NM_003331.4:c.3307A>T , LRG_121t1:c.3307A>T	NP_003322.3:p.Ser1103Cys
XM_011528245.1:c.3307A>T	XP_011526547.1:p.Ser1103Cys
XM_011528246.1:c.3010A>T	XP_011526548.1:p.Ser1004Cys
XM_011528247.1:c.3010A>T	XP_011526549.1:p.Ser1004Cys
XM_011528248.1:c.3200+481A>T	XP_011526550.1:n.3200+481A>T
XM_011528249.1:c.1981A>T	XP_011526551.1:p.Ser661Cys
XM_011528251.1:c.1564A>T	XP_011526553.1:p.Ser522Cys
XM_011528246.3:c.3010A>T	XP_011526548.1:p.Ser1004Cys
XM_011528249.2:c.1981A>T	XP_011526551.1:p.Ser661Cys
XR_001753750.1:n.3357+481A>T
XR_001753751.1:n.3859A>T
XR_002958353.1:n.4785A>T
NM_003331.5:c.3307A>T MANE Select	NP_003322.3:p.Ser1103Cys
NM_001385197.1:c.3307A>T	NP_001372126.1:p.Ser1103Cys
NM_001385198.1:c.3168+513A>T	NP_001372127.1:n.3168+513A>T
NM_001385199.1:c.3121A>T	NP_001372128.1:p.Ser1041Cys
NM_001385200.1:c.3304A>T	NP_001372129.1:p.Ser1102Cys
NM_001385201.1:c.3109A>T	NP_001372130.1:p.Ser1037Cys
NM_001385202.1:c.3223A>T	NP_001372131.1:p.Ser1075Cys
NM_001385203.1:c.3388A>T	NP_001372132.1:p.Ser1130Cys
NM_001385204.1:c.3517A>T	NP_001372133.1:p.Ser1173Cys
NM_001385205.1:c.3217A>T	NP_001372134.1:p.Ser1073Cys
NM_001385206.1:c.3181A>T	NP_001372135.1:p.Ser1061Cys
NM_001385207.1:c.3289A>T	NP_001372136.1:p.Ser1097Cys