Canonical Allele Identifier: CA403987656

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464733A>G (hg19) ; chr19:g.10354057A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354057A>G , CM000681.2:g.10354057A>G	GRCh38
NC_000019.9:g.10464733A>G , CM000681.1:g.10464733A>G	GRCh37
NC_000019.8:g.10325733A>G	NCBI36
NG_007872.1:g.31516T>C , LRG_121:g.31516T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1242T>C	ENSP00000514307.1:n.*1242T>C
ENST00000525976.6:c.2893T>C	ENSP00000434831.2:p.Cys965Arg
ENST00000527481.3:c.2893T>C	ENSP00000466340.2:p.Cys965Arg
ENST00000529370.6:n.4269T>C
ENST00000529739.2:n.3307T>C
ENST00000530829.2:c.*2444T>C	ENSP00000436826.2:n.*2444T>C
ENST00000531836.6:c.2893T>C	ENSP00000436175.2:p.Cys965Arg
ENST00000533334.2:c.*935T>C	ENSP00000432320.2:n.*935T>C
ENST00000534228.2:n.4352T>C
ENST00000699354.1:n.995T>C
ENST00000699355.1:c.*1998T>C	ENSP00000514328.1:n.*1998T>C
ENST00000699356.1:n.3307T>C
ENST00000699357.1:n.4352T>C
ENST00000699358.1:c.2893T>C	ENSP00000514329.1:p.Cys965Arg
ENST00000699359.1:c.99T>C
ENST00000699360.1:c.2893T>C	ENSP00000514331.1:p.Cys965Arg
ENST00000699368.1:c.97T>C	ENSP00000514335.1:p.Cys33Arg
ENST00000525621.6:c.2893T>C MANE Select	ENSP00000431885.1:p.Cys965Arg
ENST00000264818.10:c.2893T>C	ENSP00000264818.6:p.Cys965Arg
ENST00000524462.5:c.2338T>C	ENSP00000433203.1:p.Cys780Arg
ENST00000525621.5:c.2893T>C	ENSP00000431885.1:p.Cys965Arg
ENST00000527481.2:c.189T>C
ENST00000529412.1:n.565T>C
ENST00000529739.1:c.-434T>C	ENSP00000436155.1:n.-434T>C
ENST00000530560.5:c.322T>C	ENSP00000465291.1:p.Cys108Arg
ENST00000592137.1:n.47T>C
NM_003331.4:c.2893T>C , LRG_121t1:c.2893T>C	NP_003322.3:p.Cys965Arg
XM_011528245.1:c.2893T>C	XP_011526547.1:p.Cys965Arg
XM_011528246.1:c.2596T>C	XP_011526548.1:p.Cys866Arg
XM_011528247.1:c.2596T>C	XP_011526549.1:p.Cys866Arg
XM_011528248.1:c.2893T>C	XP_011526550.1:p.Cys965Arg
XM_011528249.1:c.1567T>C	XP_011526551.1:p.Cys523Arg
XM_011528251.1:c.1150T>C	XP_011526553.1:p.Cys384Arg
XM_011528246.3:c.2596T>C	XP_011526548.1:p.Cys866Arg
XM_011528249.2:c.1567T>C	XP_011526551.1:p.Cys523Arg
XR_001753750.1:n.3050T>C
XR_001753751.1:n.3050T>C
XR_002958353.1:n.3976T>C
NM_003331.5:c.2893T>C MANE Select	NP_003322.3:p.Cys965Arg
NM_001385197.1:c.2893T>C	NP_001372126.1:p.Cys965Arg
NM_001385198.1:c.2893T>C	NP_001372127.1:p.Cys965Arg
NM_001385199.1:c.2707T>C	NP_001372128.1:p.Cys903Arg
NM_001385200.1:c.2890T>C	NP_001372129.1:p.Cys964Arg
NM_001385201.1:c.2695T>C	NP_001372130.1:p.Cys899Arg
NM_001385202.1:c.2809T>C	NP_001372131.1:p.Cys937Arg
NM_001385203.1:c.2974T>C	NP_001372132.1:p.Cys992Arg
NM_001385204.1:c.3103T>C	NP_001372133.1:p.Cys1035Arg
NM_001385205.1:c.2803T>C	NP_001372134.1:p.Cys935Arg
NM_001385206.1:c.2767T>C	NP_001372135.1:p.Cys923Arg
NM_001385207.1:c.2875T>C	NP_001372136.1:p.Cys959Arg