Canonical Allele Identifier: CA403983223

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463169A>G (hg19) ; chr19:g.10352493A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352493A>G , CM000681.2:g.10352493A>G	GRCh38
NC_000019.9:g.10463169A>G , CM000681.1:g.10463169A>G	GRCh37
NC_000019.8:g.10324169A>G	NCBI36
NG_007872.1:g.33080T>C , LRG_121:g.33080T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1608T>C	ENSP00000514307.1:n.*1608T>C
ENST00000525976.6:c.3259T>C	ENSP00000434831.2:p.Phe1087Leu
ENST00000527481.3:c.*29T>C	ENSP00000466340.2:n.*29T>C
ENST00000529370.6:n.4635T>C
ENST00000529739.2:n.4068T>C
ENST00000530829.2:c.*2810T>C	ENSP00000436826.2:n.*2810T>C
ENST00000531836.6:c.3259T>C	ENSP00000436175.2:p.Phe1087Leu
ENST00000533334.2:c.*1242+433T>C	ENSP00000432320.2:n.*1242+433T>C
ENST00000534228.2:n.5054+433T>C
ENST00000699354.1:n.1361T>C
ENST00000699355.1:c.*2759T>C	ENSP00000514328.1:n.*2759T>C
ENST00000699356.1:n.4068T>C
ENST00000699357.1:n.5113T>C
ENST00000699358.1:c.3200+433T>C	ENSP00000514329.1:n.3200+433T>C
ENST00000699359.1:c.433T>C
ENST00000699360.1:c.3217T>C	ENSP00000514331.1:p.Phe1073Leu
ENST00000699361.1:n.293T>C
ENST00000699362.1:c.155T>C	ENSP00000514332.1:n.155T>C
ENST00000699363.1:c.155T>C	ENSP00000514333.1:n.155T>C
ENST00000699364.1:n.259T>C
ENST00000699365.1:c.328T>C	ENSP00000514334.1:p.Phe110Leu
ENST00000699366.1:n.111+1321T>C
ENST00000699367.1:n.111+1321T>C
ENST00000699368.1:c.746T>C	ENSP00000514335.1:n.746T>C
ENST00000525621.6:c.3259T>C MANE Select	ENSP00000431885.1:p.Phe1087Leu
ENST00000264818.10:c.3259T>C	ENSP00000264818.6:p.Phe1087Leu
ENST00000524462.5:c.2704T>C	ENSP00000433203.1:p.Phe902Leu
ENST00000525621.5:c.3259T>C	ENSP00000431885.1:p.Phe1087Leu
ENST00000527481.2:c.436T>C
ENST00000529422.1:n.116+529T>C
ENST00000529739.1:c.328T>C	ENSP00000436155.1:p.Phe110Leu
ENST00000530220.1:n.331+433T>C
ENST00000530560.5:c.338-1525T>C	ENSP00000465291.1:n.338-1525T>C
ENST00000592137.1:n.413T>C
NM_003331.4:c.3259T>C , LRG_121t1:c.3259T>C	NP_003322.3:p.Phe1087Leu
XM_011528245.1:c.3259T>C	XP_011526547.1:p.Phe1087Leu
XM_011528246.1:c.2962T>C	XP_011526548.1:p.Phe988Leu
XM_011528247.1:c.2962T>C	XP_011526549.1:p.Phe988Leu
XM_011528248.1:c.3200+433T>C	XP_011526550.1:n.3200+433T>C
XM_011528249.1:c.1933T>C	XP_011526551.1:p.Phe645Leu
XM_011528251.1:c.1516T>C	XP_011526553.1:p.Phe506Leu
XM_011528246.3:c.2962T>C	XP_011526548.1:p.Phe988Leu
XM_011528249.2:c.1933T>C	XP_011526551.1:p.Phe645Leu
XR_001753750.1:n.3357+433T>C
XR_001753751.1:n.3811T>C
XR_002958353.1:n.4737T>C
NM_003331.5:c.3259T>C MANE Select	NP_003322.3:p.Phe1087Leu
NM_001385197.1:c.3259T>C	NP_001372126.1:p.Phe1087Leu
NM_001385198.1:c.3168+465T>C	NP_001372127.1:n.3168+465T>C
NM_001385199.1:c.3073T>C	NP_001372128.1:p.Phe1025Leu
NM_001385200.1:c.3256T>C	NP_001372129.1:p.Phe1086Leu
NM_001385201.1:c.3061T>C	NP_001372130.1:p.Phe1021Leu
NM_001385202.1:c.3175T>C	NP_001372131.1:p.Phe1059Leu
NM_001385203.1:c.3340T>C	NP_001372132.1:p.Phe1114Leu
NM_001385204.1:c.3469T>C	NP_001372133.1:p.Phe1157Leu
NM_001385205.1:c.3169T>C	NP_001372134.1:p.Phe1057Leu
NM_001385206.1:c.3133T>C	NP_001372135.1:p.Phe1045Leu
NM_001385207.1:c.3241T>C	NP_001372136.1:p.Phe1081Leu