Canonical Allele Identifier: CA403983218

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463167G>T (hg19) ; chr19:g.10352491G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352491G>T , CM000681.2:g.10352491G>T	GRCh38
NC_000019.9:g.10463167G>T , CM000681.1:g.10463167G>T	GRCh37
NC_000019.8:g.10324167G>T	NCBI36
NG_007872.1:g.33082C>A , LRG_121:g.33082C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1610C>A	ENSP00000514307.1:n.*1610C>A
ENST00000525976.6:c.3261C>A	ENSP00000434831.2:p.Phe1087Leu
ENST00000527481.3:c.*31C>A	ENSP00000466340.2:n.*31C>A
ENST00000529370.6:n.4637C>A
ENST00000529739.2:n.4070C>A
ENST00000530829.2:c.*2812C>A	ENSP00000436826.2:n.*2812C>A
ENST00000531836.6:c.3261C>A	ENSP00000436175.2:p.Phe1087Leu
ENST00000533334.2:c.*1242+435C>A	ENSP00000432320.2:n.*1242+435C>A
ENST00000534228.2:n.5054+435C>A
ENST00000699354.1:n.1363C>A
ENST00000699355.1:c.*2761C>A	ENSP00000514328.1:n.*2761C>A
ENST00000699356.1:n.4070C>A
ENST00000699357.1:n.5115C>A
ENST00000699358.1:c.3200+435C>A	ENSP00000514329.1:n.3200+435C>A
ENST00000699359.1:c.435C>A
ENST00000699360.1:c.3219C>A	ENSP00000514331.1:p.Phe1073Leu
ENST00000699361.1:n.295C>A
ENST00000699362.1:c.157C>A	ENSP00000514332.1:n.157C>A
ENST00000699363.1:c.157C>A	ENSP00000514333.1:n.157C>A
ENST00000699364.1:n.261C>A
ENST00000699365.1:c.330C>A	ENSP00000514334.1:p.Phe110Leu
ENST00000699366.1:n.111+1323C>A
ENST00000699367.1:n.111+1323C>A
ENST00000699368.1:c.748C>A	ENSP00000514335.1:n.748C>A
ENST00000525621.6:c.3261C>A MANE Select	ENSP00000431885.1:p.Phe1087Leu
ENST00000264818.10:c.3261C>A	ENSP00000264818.6:p.Phe1087Leu
ENST00000524462.5:c.2706C>A	ENSP00000433203.1:p.Phe902Leu
ENST00000525621.5:c.3261C>A	ENSP00000431885.1:p.Phe1087Leu
ENST00000525976.5:c.2C>A
ENST00000527481.2:c.438C>A
ENST00000529422.1:n.116+531C>A
ENST00000529739.1:c.330C>A	ENSP00000436155.1:p.Phe110Leu
ENST00000530220.1:n.331+435C>A
ENST00000530560.5:c.338-1523C>A	ENSP00000465291.1:n.338-1523C>A
ENST00000592137.1:n.415C>A
NM_003331.4:c.3261C>A , LRG_121t1:c.3261C>A	NP_003322.3:p.Phe1087Leu
XM_011528245.1:c.3261C>A	XP_011526547.1:p.Phe1087Leu
XM_011528246.1:c.2964C>A	XP_011526548.1:p.Phe988Leu
XM_011528247.1:c.2964C>A	XP_011526549.1:p.Phe988Leu
XM_011528248.1:c.3200+435C>A	XP_011526550.1:n.3200+435C>A
XM_011528249.1:c.1935C>A	XP_011526551.1:p.Phe645Leu
XM_011528251.1:c.1518C>A	XP_011526553.1:p.Phe506Leu
XM_011528246.3:c.2964C>A	XP_011526548.1:p.Phe988Leu
XM_011528249.2:c.1935C>A	XP_011526551.1:p.Phe645Leu
XR_001753750.1:n.3357+435C>A
XR_001753751.1:n.3813C>A
XR_002958353.1:n.4739C>A
NM_003331.5:c.3261C>A MANE Select	NP_003322.3:p.Phe1087Leu
NM_001385197.1:c.3261C>A	NP_001372126.1:p.Phe1087Leu
NM_001385198.1:c.3168+467C>A	NP_001372127.1:n.3168+467C>A
NM_001385199.1:c.3075C>A	NP_001372128.1:p.Phe1025Leu
NM_001385200.1:c.3258C>A	NP_001372129.1:p.Phe1086Leu
NM_001385201.1:c.3063C>A	NP_001372130.1:p.Phe1021Leu
NM_001385202.1:c.3177C>A	NP_001372131.1:p.Phe1059Leu
NM_001385203.1:c.3342C>A	NP_001372132.1:p.Phe1114Leu
NM_001385204.1:c.3471C>A	NP_001372133.1:p.Phe1157Leu
NM_001385205.1:c.3171C>A	NP_001372134.1:p.Phe1057Leu
NM_001385206.1:c.3135C>A	NP_001372135.1:p.Phe1045Leu
NM_001385207.1:c.3243C>A	NP_001372136.1:p.Phe1081Leu