Canonical Allele Identifier: CA403987958

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464772G>T (hg19) ; chr19:g.10354096G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354096G>T , CM000681.2:g.10354096G>T	GRCh38
NC_000019.9:g.10464772G>T , CM000681.1:g.10464772G>T	GRCh37
NC_000019.8:g.10325772G>T	NCBI36
NG_007872.1:g.31477C>A , LRG_121:g.31477C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1203C>A	ENSP00000514307.1:n.*1203C>A
ENST00000525976.6:c.2854C>A	ENSP00000434831.2:p.Arg952Ser
ENST00000527481.3:c.2854C>A	ENSP00000466340.2:p.Arg952Ser
ENST00000529370.6:n.4230C>A
ENST00000529739.2:n.3268C>A
ENST00000530829.2:c.*2405C>A	ENSP00000436826.2:n.*2405C>A
ENST00000531836.6:c.2854C>A	ENSP00000436175.2:p.Arg952Ser
ENST00000533334.2:c.*896C>A	ENSP00000432320.2:n.*896C>A
ENST00000534228.2:n.4313C>A
ENST00000699354.1:n.956C>A
ENST00000699355.1:c.*1959C>A	ENSP00000514328.1:n.*1959C>A
ENST00000699356.1:n.3268C>A
ENST00000699357.1:n.4313C>A
ENST00000699358.1:c.2854C>A	ENSP00000514329.1:p.Arg952Ser
ENST00000699359.1:c.60C>A
ENST00000699360.1:c.2854C>A	ENSP00000514331.1:p.Arg952Ser
ENST00000699368.1:c.58C>A	ENSP00000514335.1:p.Arg20Ser
ENST00000525621.6:c.2854C>A MANE Select	ENSP00000431885.1:p.Arg952Ser
ENST00000264818.10:c.2854C>A	ENSP00000264818.6:p.Arg952Ser
ENST00000524462.5:c.2299C>A	ENSP00000433203.1:p.Arg767Ser
ENST00000525621.5:c.2854C>A	ENSP00000431885.1:p.Arg952Ser
ENST00000527481.2:c.150C>A
ENST00000529412.1:n.526C>A
ENST00000530560.5:c.283C>A	ENSP00000465291.1:p.Arg95Ser
ENST00000592137.1:n.8C>A
NM_003331.4:c.2854C>A , LRG_121t1:c.2854C>A	NP_003322.3:p.Arg952Ser
XM_011528245.1:c.2854C>A	XP_011526547.1:p.Arg952Ser
XM_011528246.1:c.2557C>A	XP_011526548.1:p.Arg853Ser
XM_011528247.1:c.2557C>A	XP_011526549.1:p.Arg853Ser
XM_011528248.1:c.2854C>A	XP_011526550.1:p.Arg952Ser
XM_011528249.1:c.1528C>A	XP_011526551.1:p.Arg510Ser
XM_011528251.1:c.1111C>A	XP_011526553.1:p.Arg371Ser
XM_011528246.3:c.2557C>A	XP_011526548.1:p.Arg853Ser
XM_011528249.2:c.1528C>A	XP_011526551.1:p.Arg510Ser
XR_001753750.1:n.3011C>A
XR_001753751.1:n.3011C>A
XR_002958353.1:n.3937C>A
NM_003331.5:c.2854C>A MANE Select	NP_003322.3:p.Arg952Ser
NM_001385197.1:c.2854C>A	NP_001372126.1:p.Arg952Ser
NM_001385198.1:c.2854C>A	NP_001372127.1:p.Arg952Ser
NM_001385199.1:c.2668C>A	NP_001372128.1:p.Arg890Ser
NM_001385200.1:c.2851C>A	NP_001372129.1:p.Arg951Ser
NM_001385201.1:c.2656C>A	NP_001372130.1:p.Arg886Ser
NM_001385202.1:c.2770C>A	NP_001372131.1:p.Arg924Ser
NM_001385203.1:c.2935C>A	NP_001372132.1:p.Arg979Ser
NM_001385204.1:c.3064C>A	NP_001372133.1:p.Arg1022Ser
NM_001385205.1:c.2764C>A	NP_001372134.1:p.Arg922Ser
NM_001385206.1:c.2728C>A	NP_001372135.1:p.Arg910Ser
NM_001385207.1:c.2836C>A	NP_001372136.1:p.Arg946Ser