Canonical Allele Identifier: CA403988447

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464818G>T (hg19) ; chr19:g.10354142G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354142G>T , CM000681.2:g.10354142G>T	GRCh38
NC_000019.9:g.10464818G>T , CM000681.1:g.10464818G>T	GRCh37
NC_000019.8:g.10325818G>T	NCBI36
NG_007872.1:g.31431C>A , LRG_121:g.31431C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1157C>A	ENSP00000514307.1:n.*1157C>A
ENST00000525976.6:c.2808C>A	ENSP00000434831.2:p.Cys936Ter
ENST00000527481.3:c.2808C>A	ENSP00000466340.2:p.Cys936Ter
ENST00000529370.6:n.4184C>A
ENST00000529739.2:n.3222C>A
ENST00000530829.2:c.*2359C>A	ENSP00000436826.2:n.*2359C>A
ENST00000531836.6:c.2808C>A	ENSP00000436175.2:p.Cys936Ter
ENST00000533334.2:c.*850C>A	ENSP00000432320.2:n.*850C>A
ENST00000534228.2:n.4267C>A
ENST00000699354.1:n.910C>A
ENST00000699355.1:c.*1913C>A	ENSP00000514328.1:n.*1913C>A
ENST00000699356.1:n.3222C>A
ENST00000699357.1:n.4267C>A
ENST00000699358.1:c.2808C>A	ENSP00000514329.1:p.Cys936Ter
ENST00000699359.1:c.14C>A
ENST00000699360.1:c.2808C>A	ENSP00000514331.1:p.Cys936Ter
ENST00000699368.1:c.12C>A	ENSP00000514335.1:p.Cys4Ter
ENST00000525621.6:c.2808C>A MANE Select	ENSP00000431885.1:p.Cys936Ter
ENST00000264818.10:c.2808C>A	ENSP00000264818.6:p.Cys936Ter
ENST00000524462.5:c.2253C>A	ENSP00000433203.1:p.Cys751Ter
ENST00000525621.5:c.2808C>A	ENSP00000431885.1:p.Cys936Ter
ENST00000527481.2:c.104C>A
ENST00000529412.1:n.480C>A
ENST00000530560.5:c.237C>A	ENSP00000465291.1:p.Cys79Ter
NM_003331.4:c.2808C>A , LRG_121t1:c.2808C>A	NP_003322.3:p.Cys936Ter
XM_011528245.1:c.2808C>A	XP_011526547.1:p.Cys936Ter
XM_011528246.1:c.2511C>A	XP_011526548.1:p.Cys837Ter
XM_011528247.1:c.2511C>A	XP_011526549.1:p.Cys837Ter
XM_011528248.1:c.2808C>A	XP_011526550.1:p.Cys936Ter
XM_011528249.1:c.1482C>A	XP_011526551.1:p.Cys494Ter
XM_011528251.1:c.1065C>A	XP_011526553.1:p.Cys355Ter
XM_011528246.3:c.2511C>A	XP_011526548.1:p.Cys837Ter
XM_011528249.2:c.1482C>A	XP_011526551.1:p.Cys494Ter
XR_001753750.1:n.2965C>A
XR_001753751.1:n.2965C>A
XR_002958353.1:n.3891C>A
NM_003331.5:c.2808C>A MANE Select	NP_003322.3:p.Cys936Ter
NM_001385197.1:c.2808C>A	NP_001372126.1:p.Cys936Ter
NM_001385198.1:c.2808C>A	NP_001372127.1:p.Cys936Ter
NM_001385199.1:c.2622C>A	NP_001372128.1:p.Cys874Ter
NM_001385200.1:c.2805C>A	NP_001372129.1:p.Cys935Ter
NM_001385201.1:c.2610C>A	NP_001372130.1:p.Cys870Ter
NM_001385202.1:c.2724C>A	NP_001372131.1:p.Cys908Ter
NM_001385203.1:c.2889C>A	NP_001372132.1:p.Cys963Ter
NM_001385204.1:c.3018C>A	NP_001372133.1:p.Cys1006Ter
NM_001385205.1:c.2718C>A	NP_001372134.1:p.Cys906Ter
NM_001385206.1:c.2682C>A	NP_001372135.1:p.Cys894Ter
NM_001385207.1:c.2790C>A	NP_001372136.1:p.Cys930Ter