Canonical Allele Identifier: CA403983204

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463160T>A (hg19) ; chr19:g.10352484T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352484T>A , CM000681.2:g.10352484T>A	GRCh38
NC_000019.9:g.10463160T>A , CM000681.1:g.10463160T>A	GRCh37
NC_000019.8:g.10324160T>A	NCBI36
NG_007872.1:g.33089A>T , LRG_121:g.33089A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1617A>T	ENSP00000514307.1:n.*1617A>T
ENST00000525976.6:c.3268A>T	ENSP00000434831.2:p.Thr1090Ser
ENST00000527481.3:c.*38A>T	ENSP00000466340.2:n.*38A>T
ENST00000529370.6:n.4644A>T
ENST00000529739.2:n.4077A>T
ENST00000530829.2:c.*2819A>T	ENSP00000436826.2:n.*2819A>T
ENST00000531836.6:c.3268A>T	ENSP00000436175.2:p.Thr1090Ser
ENST00000533334.2:c.*1242+442A>T	ENSP00000432320.2:n.*1242+442A>T
ENST00000534228.2:n.5054+442A>T
ENST00000699354.1:n.1370A>T
ENST00000699355.1:c.*2768A>T	ENSP00000514328.1:n.*2768A>T
ENST00000699356.1:n.4077A>T
ENST00000699357.1:n.5122A>T
ENST00000699358.1:c.3200+442A>T	ENSP00000514329.1:n.3200+442A>T
ENST00000699359.1:c.442A>T
ENST00000699360.1:c.3226A>T	ENSP00000514331.1:p.Thr1076Ser
ENST00000699361.1:n.302A>T
ENST00000699362.1:c.164A>T	ENSP00000514332.1:n.164A>T
ENST00000699363.1:c.164A>T	ENSP00000514333.1:n.164A>T
ENST00000699364.1:n.268A>T
ENST00000699365.1:c.337A>T	ENSP00000514334.1:p.Thr113Ser
ENST00000699366.1:n.111+1330A>T
ENST00000699367.1:n.112-1322A>T
ENST00000699368.1:c.755A>T	ENSP00000514335.1:n.755A>T
ENST00000525621.6:c.3268A>T MANE Select	ENSP00000431885.1:p.Thr1090Ser
ENST00000264818.10:c.3268A>T	ENSP00000264818.6:p.Thr1090Ser
ENST00000524462.5:c.2713A>T	ENSP00000433203.1:p.Thr905Ser
ENST00000525621.5:c.3268A>T	ENSP00000431885.1:p.Thr1090Ser
ENST00000525976.5:c.9A>T
ENST00000527481.2:c.445A>T
ENST00000529422.1:n.116+538A>T
ENST00000529739.1:c.337A>T	ENSP00000436155.1:p.Thr113Ser
ENST00000530220.1:n.331+442A>T
ENST00000530560.5:c.338-1516A>T	ENSP00000465291.1:n.338-1516A>T
ENST00000592137.1:n.422A>T
NM_003331.4:c.3268A>T , LRG_121t1:c.3268A>T	NP_003322.3:p.Thr1090Ser
XM_011528245.1:c.3268A>T	XP_011526547.1:p.Thr1090Ser
XM_011528246.1:c.2971A>T	XP_011526548.1:p.Thr991Ser
XM_011528247.1:c.2971A>T	XP_011526549.1:p.Thr991Ser
XM_011528248.1:c.3200+442A>T	XP_011526550.1:n.3200+442A>T
XM_011528249.1:c.1942A>T	XP_011526551.1:p.Thr648Ser
XM_011528251.1:c.1525A>T	XP_011526553.1:p.Thr509Ser
XM_011528246.3:c.2971A>T	XP_011526548.1:p.Thr991Ser
XM_011528249.2:c.1942A>T	XP_011526551.1:p.Thr648Ser
XR_001753750.1:n.3357+442A>T
XR_001753751.1:n.3820A>T
XR_002958353.1:n.4746A>T
NM_003331.5:c.3268A>T MANE Select	NP_003322.3:p.Thr1090Ser
NM_001385197.1:c.3268A>T	NP_001372126.1:p.Thr1090Ser
NM_001385198.1:c.3168+474A>T	NP_001372127.1:n.3168+474A>T
NM_001385199.1:c.3082A>T	NP_001372128.1:p.Thr1028Ser
NM_001385200.1:c.3265A>T	NP_001372129.1:p.Thr1089Ser
NM_001385201.1:c.3070A>T	NP_001372130.1:p.Thr1024Ser
NM_001385202.1:c.3184A>T	NP_001372131.1:p.Thr1062Ser
NM_001385203.1:c.3349A>T	NP_001372132.1:p.Thr1117Ser
NM_001385204.1:c.3478A>T	NP_001372133.1:p.Thr1160Ser
NM_001385205.1:c.3178A>T	NP_001372134.1:p.Thr1060Ser
NM_001385206.1:c.3142A>T	NP_001372135.1:p.Thr1048Ser
NM_001385207.1:c.3250A>T	NP_001372136.1:p.Thr1084Ser