Canonical Allele Identifier: CA403987609

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464725C>G (hg19) ; chr19:g.10354049C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354049C>G , CM000681.2:g.10354049C>G	GRCh38
NC_000019.9:g.10464725C>G , CM000681.1:g.10464725C>G	GRCh37
NC_000019.8:g.10325725C>G	NCBI36
NG_007872.1:g.31524G>C , LRG_121:g.31524G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1250G>C	ENSP00000514307.1:n.*1250G>C
ENST00000525976.6:c.2901G>C	ENSP00000434831.2:p.Glu967Asp
ENST00000527481.3:c.2901G>C	ENSP00000466340.2:p.Glu967Asp
ENST00000529370.6:n.4277G>C
ENST00000529739.2:n.3315G>C
ENST00000530829.2:c.*2452G>C	ENSP00000436826.2:n.*2452G>C
ENST00000531836.6:c.2901G>C	ENSP00000436175.2:p.Glu967Asp
ENST00000533334.2:c.*943G>C	ENSP00000432320.2:n.*943G>C
ENST00000534228.2:n.4360G>C
ENST00000699354.1:n.1003G>C
ENST00000699355.1:c.*2006G>C	ENSP00000514328.1:n.*2006G>C
ENST00000699356.1:n.3315G>C
ENST00000699357.1:n.4360G>C
ENST00000699358.1:c.2901G>C	ENSP00000514329.1:p.Glu967Asp
ENST00000699359.1:c.107G>C
ENST00000699360.1:c.2901G>C	ENSP00000514331.1:p.Glu967Asp
ENST00000699368.1:c.105G>C	ENSP00000514335.1:p.Glu35Asp
ENST00000525621.6:c.2901G>C MANE Select	ENSP00000431885.1:p.Glu967Asp
ENST00000264818.10:c.2901G>C	ENSP00000264818.6:p.Glu967Asp
ENST00000524462.5:c.2346G>C	ENSP00000433203.1:p.Glu782Asp
ENST00000525621.5:c.2901G>C	ENSP00000431885.1:p.Glu967Asp
ENST00000527481.2:c.197G>C
ENST00000529412.1:n.573G>C
ENST00000529739.1:c.-426G>C	ENSP00000436155.1:n.-426G>C
ENST00000530560.5:c.330G>C	ENSP00000465291.1:p.Glu110Asp
ENST00000592137.1:n.55G>C
NM_003331.4:c.2901G>C , LRG_121t1:c.2901G>C	NP_003322.3:p.Glu967Asp
XM_011528245.1:c.2901G>C	XP_011526547.1:p.Glu967Asp
XM_011528246.1:c.2604G>C	XP_011526548.1:p.Glu868Asp
XM_011528247.1:c.2604G>C	XP_011526549.1:p.Glu868Asp
XM_011528248.1:c.2901G>C	XP_011526550.1:p.Glu967Asp
XM_011528249.1:c.1575G>C	XP_011526551.1:p.Glu525Asp
XM_011528251.1:c.1158G>C	XP_011526553.1:p.Glu386Asp
XM_011528246.3:c.2604G>C	XP_011526548.1:p.Glu868Asp
XM_011528249.2:c.1575G>C	XP_011526551.1:p.Glu525Asp
XR_001753750.1:n.3058G>C
XR_001753751.1:n.3058G>C
XR_002958353.1:n.3984G>C
NM_003331.5:c.2901G>C MANE Select	NP_003322.3:p.Glu967Asp
NM_001385197.1:c.2901G>C	NP_001372126.1:p.Glu967Asp
NM_001385198.1:c.2901G>C	NP_001372127.1:p.Glu967Asp
NM_001385199.1:c.2715G>C	NP_001372128.1:p.Glu905Asp
NM_001385200.1:c.2898G>C	NP_001372129.1:p.Glu966Asp
NM_001385201.1:c.2703G>C	NP_001372130.1:p.Glu901Asp
NM_001385202.1:c.2817G>C	NP_001372131.1:p.Glu939Asp
NM_001385203.1:c.2982G>C	NP_001372132.1:p.Glu994Asp
NM_001385204.1:c.3111G>C	NP_001372133.1:p.Glu1037Asp
NM_001385205.1:c.2811G>C	NP_001372134.1:p.Glu937Asp
NM_001385206.1:c.2775G>C	NP_001372135.1:p.Glu925Asp
NM_001385207.1:c.2883G>C	NP_001372136.1:p.Glu961Asp