Canonical Allele Identifier: CA403995257

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10468471T>A (hg19) ; chr19:g.10357795T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10357795T>A , CM000681.2:g.10357795T>A	GRCh38
NC_000019.9:g.10468471T>A , CM000681.1:g.10468471T>A	GRCh37
NC_000019.8:g.10329471T>A	NCBI36
NG_007872.1:g.27778A>T , LRG_121:g.27778A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*784A>T	ENSP00000514307.1:n.*784A>T
ENST00000525976.6:c.2435A>T	ENSP00000434831.2:p.Glu812Val
ENST00000527481.3:c.2435A>T	ENSP00000466340.2:p.Glu812Val
ENST00000529370.6:n.2766A>T
ENST00000529739.2:n.2849A>T
ENST00000530829.2:c.*1986A>T	ENSP00000436826.2:n.*1986A>T
ENST00000531836.6:c.2435A>T	ENSP00000436175.2:p.Glu812Val
ENST00000533334.2:c.*477A>T	ENSP00000432320.2:n.*477A>T
ENST00000534228.2:n.2849A>T
ENST00000699354.1:n.537A>T
ENST00000699355.1:c.*495A>T	ENSP00000514328.1:n.*495A>T
ENST00000699356.1:n.2849A>T
ENST00000699357.1:n.2849A>T
ENST00000699358.1:c.2435A>T	ENSP00000514329.1:p.Glu812Val
ENST00000699360.1:c.2435A>T	ENSP00000514331.1:p.Glu812Val
ENST00000525621.6:c.2435A>T MANE Select	ENSP00000431885.1:p.Glu812Val
ENST00000264818.10:c.2435A>T	ENSP00000264818.6:p.Glu812Val
ENST00000524462.5:c.1880A>T	ENSP00000433203.1:p.Glu627Val
ENST00000525621.5:c.2435A>T	ENSP00000431885.1:p.Glu812Val
ENST00000529370.5:c.2435A>T	ENSP00000432728.1:p.Glu812Val
ENST00000529412.1:n.107A>T
ENST00000533334.1:c.724A>T
NM_003331.4:c.2435A>T , LRG_121t1:c.2435A>T	NP_003322.3:p.Glu812Val
XM_011528245.1:c.2435A>T	XP_011526547.1:p.Glu812Val
XM_011528246.1:c.2138A>T	XP_011526548.1:p.Glu713Val
XM_011528247.1:c.2138A>T	XP_011526549.1:p.Glu713Val
XM_011528248.1:c.2435A>T	XP_011526550.1:p.Glu812Val
XM_011528249.1:c.1109A>T	XP_011526551.1:p.Glu370Val
XM_011528251.1:c.692A>T	XP_011526553.1:p.Glu231Val
XM_011528246.3:c.2138A>T	XP_011526548.1:p.Glu713Val
XM_011528249.2:c.1109A>T	XP_011526551.1:p.Glu370Val
XR_001753750.1:n.2592A>T
XR_001753751.1:n.2592A>T
XR_002958353.1:n.2473A>T
NM_003331.5:c.2435A>T MANE Select	NP_003322.3:p.Glu812Val
NM_001385197.1:c.2435A>T	NP_001372126.1:p.Glu812Val
NM_001385198.1:c.2435A>T	NP_001372127.1:p.Glu812Val
NM_001385199.1:c.2249A>T	NP_001372128.1:p.Glu750Val
NM_001385200.1:c.2435A>T	NP_001372129.1:p.Glu812Val
NM_001385201.1:c.2237A>T	NP_001372130.1:p.Glu746Val
NM_001385202.1:c.2351A>T	NP_001372131.1:p.Glu784Val
NM_001385203.1:c.2435A>T	NP_001372132.1:p.Glu812Val
NM_001385204.1:c.2435A>T	NP_001372133.1:p.Glu812Val
NM_001385205.1:c.2345A>T	NP_001372134.1:p.Glu782Val
NM_001385206.1:c.2309A>T	NP_001372135.1:p.Glu770Val
NM_001385207.1:c.2417A>T	NP_001372136.1:p.Glu806Val