Canonical Allele Identifier: CA403989165

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464891C>G (hg19) ; chr19:g.10354215C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354215C>G , CM000681.2:g.10354215C>G	GRCh38
NC_000019.9:g.10464891C>G , CM000681.1:g.10464891C>G	GRCh37
NC_000019.8:g.10325891C>G	NCBI36
NG_007872.1:g.31358G>C , LRG_121:g.31358G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1084G>C	ENSP00000514307.1:n.*1084G>C
ENST00000525976.6:c.2735G>C	ENSP00000434831.2:p.Ser912Thr
ENST00000527481.3:c.2735G>C	ENSP00000466340.2:p.Ser912Thr
ENST00000529370.6:n.4111G>C
ENST00000529739.2:n.3149G>C
ENST00000530829.2:c.*2286G>C	ENSP00000436826.2:n.*2286G>C
ENST00000531836.6:c.2735G>C	ENSP00000436175.2:p.Ser912Thr
ENST00000533334.2:c.*777G>C	ENSP00000432320.2:n.*777G>C
ENST00000534228.2:n.4194G>C
ENST00000699354.1:n.837G>C
ENST00000699355.1:c.*1840G>C	ENSP00000514328.1:n.*1840G>C
ENST00000699356.1:n.3149G>C
ENST00000699357.1:n.4194G>C
ENST00000699358.1:c.2735G>C	ENSP00000514329.1:p.Ser912Thr
ENST00000699360.1:c.2735G>C	ENSP00000514331.1:p.Ser912Thr
ENST00000525621.6:c.2735G>C MANE Select	ENSP00000431885.1:p.Ser912Thr
ENST00000264818.10:c.2735G>C	ENSP00000264818.6:p.Ser912Thr
ENST00000524462.5:c.2180G>C	ENSP00000433203.1:p.Ser727Thr
ENST00000525621.5:c.2735G>C	ENSP00000431885.1:p.Ser912Thr
ENST00000527481.2:c.31G>C
ENST00000529412.1:n.407G>C
ENST00000530560.5:c.164G>C	ENSP00000465291.1:p.Ser55Thr
NM_003331.4:c.2735G>C , LRG_121t1:c.2735G>C	NP_003322.3:p.Ser912Thr
XM_011528245.1:c.2735G>C	XP_011526547.1:p.Ser912Thr
XM_011528246.1:c.2438G>C	XP_011526548.1:p.Ser813Thr
XM_011528247.1:c.2438G>C	XP_011526549.1:p.Ser813Thr
XM_011528248.1:c.2735G>C	XP_011526550.1:p.Ser912Thr
XM_011528249.1:c.1409G>C	XP_011526551.1:p.Ser470Thr
XM_011528251.1:c.992G>C	XP_011526553.1:p.Ser331Thr
XM_011528246.3:c.2438G>C	XP_011526548.1:p.Ser813Thr
XM_011528249.2:c.1409G>C	XP_011526551.1:p.Ser470Thr
XR_001753750.1:n.2892G>C
XR_001753751.1:n.2892G>C
XR_002958353.1:n.3818G>C
NM_003331.5:c.2735G>C MANE Select	NP_003322.3:p.Ser912Thr
NM_001385197.1:c.2735G>C	NP_001372126.1:p.Ser912Thr
NM_001385198.1:c.2735G>C	NP_001372127.1:p.Ser912Thr
NM_001385199.1:c.2549G>C	NP_001372128.1:p.Ser850Thr
NM_001385200.1:c.2732G>C	NP_001372129.1:p.Ser911Thr
NM_001385201.1:c.2537G>C	NP_001372130.1:p.Ser846Thr
NM_001385202.1:c.2651G>C	NP_001372131.1:p.Ser884Thr
NM_001385203.1:c.2816G>C	NP_001372132.1:p.Ser939Thr
NM_001385204.1:c.2945G>C	NP_001372133.1:p.Ser982Thr
NM_001385205.1:c.2645G>C	NP_001372134.1:p.Ser882Thr
NM_001385206.1:c.2609G>C	NP_001372135.1:p.Ser870Thr
NM_001385207.1:c.2717G>C	NP_001372136.1:p.Ser906Thr