Canonical Allele Identifier: CA403987997

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464778T>A (hg19) ; chr19:g.10354102T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354102T>A , CM000681.2:g.10354102T>A	GRCh38
NC_000019.9:g.10464778T>A , CM000681.1:g.10464778T>A	GRCh37
NC_000019.8:g.10325778T>A	NCBI36
NG_007872.1:g.31471A>T , LRG_121:g.31471A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1197A>T	ENSP00000514307.1:n.*1197A>T
ENST00000525976.6:c.2848A>T	ENSP00000434831.2:p.Ile950Phe
ENST00000527481.3:c.2848A>T	ENSP00000466340.2:p.Ile950Phe
ENST00000529370.6:n.4224A>T
ENST00000529739.2:n.3262A>T
ENST00000530829.2:c.*2399A>T	ENSP00000436826.2:n.*2399A>T
ENST00000531836.6:c.2848A>T	ENSP00000436175.2:p.Ile950Phe
ENST00000533334.2:c.*890A>T	ENSP00000432320.2:n.*890A>T
ENST00000534228.2:n.4307A>T
ENST00000699354.1:n.950A>T
ENST00000699355.1:c.*1953A>T	ENSP00000514328.1:n.*1953A>T
ENST00000699356.1:n.3262A>T
ENST00000699357.1:n.4307A>T
ENST00000699358.1:c.2848A>T	ENSP00000514329.1:p.Ile950Phe
ENST00000699359.1:c.54A>T
ENST00000699360.1:c.2848A>T	ENSP00000514331.1:p.Ile950Phe
ENST00000699368.1:c.52A>T	ENSP00000514335.1:p.Ile18Phe
ENST00000525621.6:c.2848A>T MANE Select	ENSP00000431885.1:p.Ile950Phe
ENST00000264818.10:c.2848A>T	ENSP00000264818.6:p.Ile950Phe
ENST00000524462.5:c.2293A>T	ENSP00000433203.1:p.Ile765Phe
ENST00000525621.5:c.2848A>T	ENSP00000431885.1:p.Ile950Phe
ENST00000527481.2:c.144A>T
ENST00000529412.1:n.520A>T
ENST00000530560.5:c.277A>T	ENSP00000465291.1:p.Ile93Phe
ENST00000592137.1:n.2A>T
NM_003331.4:c.2848A>T , LRG_121t1:c.2848A>T	NP_003322.3:p.Ile950Phe
XM_011528245.1:c.2848A>T	XP_011526547.1:p.Ile950Phe
XM_011528246.1:c.2551A>T	XP_011526548.1:p.Ile851Phe
XM_011528247.1:c.2551A>T	XP_011526549.1:p.Ile851Phe
XM_011528248.1:c.2848A>T	XP_011526550.1:p.Ile950Phe
XM_011528249.1:c.1522A>T	XP_011526551.1:p.Ile508Phe
XM_011528251.1:c.1105A>T	XP_011526553.1:p.Ile369Phe
XM_011528246.3:c.2551A>T	XP_011526548.1:p.Ile851Phe
XM_011528249.2:c.1522A>T	XP_011526551.1:p.Ile508Phe
XR_001753750.1:n.3005A>T
XR_001753751.1:n.3005A>T
XR_002958353.1:n.3931A>T
NM_003331.5:c.2848A>T MANE Select	NP_003322.3:p.Ile950Phe
NM_001385197.1:c.2848A>T	NP_001372126.1:p.Ile950Phe
NM_001385198.1:c.2848A>T	NP_001372127.1:p.Ile950Phe
NM_001385199.1:c.2662A>T	NP_001372128.1:p.Ile888Phe
NM_001385200.1:c.2845A>T	NP_001372129.1:p.Ile949Phe
NM_001385201.1:c.2650A>T	NP_001372130.1:p.Ile884Phe
NM_001385202.1:c.2764A>T	NP_001372131.1:p.Ile922Phe
NM_001385203.1:c.2929A>T	NP_001372132.1:p.Ile977Phe
NM_001385204.1:c.3058A>T	NP_001372133.1:p.Ile1020Phe
NM_001385205.1:c.2758A>T	NP_001372134.1:p.Ile920Phe
NM_001385206.1:c.2722A>T	NP_001372135.1:p.Ile908Phe
NM_001385207.1:c.2830A>T	NP_001372136.1:p.Ile944Phe