Canonical Allele Identifier: CA2322387981

Gene: TYK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354055_10354056delinsGC , CM000681.2:g.10354055_10354056delinsGC	GRCh38
NC_000019.9:g.10464731_10464732delinsGC , CM000681.1:g.10464731_10464732delinsGC	GRCh37
NC_000019.8:g.10325731_10325732delinsGC	NCBI36
NG_007872.1:g.31517_31518delinsGC , LRG_121:g.31517_31518delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1243_*1244delinsGC	ENSP00000514307.1:n.*1243_*1244delinsGC
ENST00000525976.6:c.2894_2895delinsGC	ENSP00000434831.2:p.Cys965=
ENST00000527481.3:c.2894_2895delinsGC	ENSP00000466340.2:p.Cys965=
ENST00000529370.6:n.4270_4271delinsGC
ENST00000529739.2:n.3308_3309delinsGC
ENST00000530829.2:c.*2445_*2446delinsGC	ENSP00000436826.2:n.*2445_*2446delinsGC
ENST00000531836.6:c.2894_2895delinsGC	ENSP00000436175.2:p.Cys965=
ENST00000533334.2:c.*936_*937delinsGC	ENSP00000432320.2:n.*936_*937delinsGC
ENST00000534228.2:n.4353_4354delinsGC
ENST00000699354.1:n.996_997delinsGC
ENST00000699355.1:c.*1999_*2000delinsGC	ENSP00000514328.1:n.*1999_*2000delinsGC
ENST00000699356.1:n.3308_3309delinsGC
ENST00000699357.1:n.4353_4354delinsGC
ENST00000699358.1:c.2894_2895delinsGC	ENSP00000514329.1:p.Cys965=
ENST00000699359.1:c.100_101delinsGC
ENST00000699360.1:c.2894_2895delinsGC	ENSP00000514331.1:p.Cys965=
ENST00000699368.1:c.98_99delinsGC	ENSP00000514335.1:p.Cys33=
ENST00000525621.6:c.2894_2895delinsGC MANE Select	ENSP00000431885.1:p.Cys965=
ENST00000264818.10:c.2894_2895delinsGC	ENSP00000264818.6:p.Cys965=
ENST00000524462.5:c.2339_2340delinsGC	ENSP00000433203.1:p.Cys780=
ENST00000525621.5:c.2894_2895delinsGC	ENSP00000431885.1:p.Cys965=
ENST00000527481.2:c.190_191delinsGC
ENST00000529412.1:n.566_567delinsGC
ENST00000529739.1:c.-433_-432delinsGC	ENSP00000436155.1:n.-433_-432delinsGC
ENST00000530560.5:c.323_324delinsGC	ENSP00000465291.1:p.Cys108=
ENST00000592137.1:n.48_49delinsGC
NM_003331.4:c.2894_2895delinsGC , LRG_121t1:c.2894_2895delinsGC	NP_003322.3:p.Cys965=
XM_011528245.1:c.2894_2895delinsGC	XP_011526547.1:p.Cys965=
XM_011528246.1:c.2597_2598delinsGC	XP_011526548.1:p.Cys866=
XM_011528247.1:c.2597_2598delinsGC	XP_011526549.1:p.Cys866=
XM_011528248.1:c.2894_2895delinsGC	XP_011526550.1:p.Cys965=
XM_011528249.1:c.1568_1569delinsGC	XP_011526551.1:p.Cys523=
XM_011528251.1:c.1151_1152delinsGC	XP_011526553.1:p.Cys384=
XM_011528246.3:c.2597_2598delinsGC	XP_011526548.1:p.Cys866=
XM_011528249.2:c.1568_1569delinsGC	XP_011526551.1:p.Cys523=
XR_001753750.1:n.3051_3052delinsGC
XR_001753751.1:n.3051_3052delinsGC
XR_002958353.1:n.3977_3978delinsGC
NM_003331.5:c.2894_2895delinsGC MANE Select	NP_003322.3:p.Cys965=
NM_001385197.1:c.2894_2895delinsGC	NP_001372126.1:p.Cys965=
NM_001385198.1:c.2894_2895delinsGC	NP_001372127.1:p.Cys965=
NM_001385199.1:c.2708_2709delinsGC	NP_001372128.1:p.Cys903=
NM_001385200.1:c.2891_2892delinsGC	NP_001372129.1:p.Cys964=
NM_001385201.1:c.2696_2697delinsGC	NP_001372130.1:p.Cys899=
NM_001385202.1:c.2810_2811delinsGC	NP_001372131.1:p.Cys937=
NM_001385203.1:c.2975_2976delinsGC	NP_001372132.1:p.Cys992=
NM_001385204.1:c.3104_3105delinsGC	NP_001372133.1:p.Cys1035=
NM_001385205.1:c.2804_2805delinsGC	NP_001372134.1:p.Cys935=
NM_001385206.1:c.2768_2769delinsGC	NP_001372135.1:p.Cys923=
NM_001385207.1:c.2876_2877delinsGC	NP_001372136.1:p.Cys959=