Canonical Allele Identifier: CA403988614

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464840A>T (hg19) ; chr19:g.10354164A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354164A>T , CM000681.2:g.10354164A>T	GRCh38
NC_000019.9:g.10464840A>T , CM000681.1:g.10464840A>T	GRCh37
NC_000019.8:g.10325840A>T	NCBI36
NG_007872.1:g.31409T>A , LRG_121:g.31409T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1135T>A	ENSP00000514307.1:n.*1135T>A
ENST00000525976.6:c.2786T>A	ENSP00000434831.2:p.Val929Glu
ENST00000527481.3:c.2786T>A	ENSP00000466340.2:p.Val929Glu
ENST00000529370.6:n.4162T>A
ENST00000529739.2:n.3200T>A
ENST00000530829.2:c.*2337T>A	ENSP00000436826.2:n.*2337T>A
ENST00000531836.6:c.2786T>A	ENSP00000436175.2:p.Val929Glu
ENST00000533334.2:c.*828T>A	ENSP00000432320.2:n.*828T>A
ENST00000534228.2:n.4245T>A
ENST00000699354.1:n.888T>A
ENST00000699355.1:c.*1891T>A	ENSP00000514328.1:n.*1891T>A
ENST00000699356.1:n.3200T>A
ENST00000699357.1:n.4245T>A
ENST00000699358.1:c.2786T>A	ENSP00000514329.1:p.Val929Glu
ENST00000699360.1:c.2786T>A	ENSP00000514331.1:p.Val929Glu
ENST00000525621.6:c.2786T>A MANE Select	ENSP00000431885.1:p.Val929Glu
ENST00000264818.10:c.2786T>A	ENSP00000264818.6:p.Val929Glu
ENST00000524462.5:c.2231T>A	ENSP00000433203.1:p.Val744Glu
ENST00000525621.5:c.2786T>A	ENSP00000431885.1:p.Val929Glu
ENST00000527481.2:c.82T>A
ENST00000529412.1:n.458T>A
ENST00000530560.5:c.215T>A	ENSP00000465291.1:p.Val72Glu
NM_003331.4:c.2786T>A , LRG_121t1:c.2786T>A	NP_003322.3:p.Val929Glu
XM_011528245.1:c.2786T>A	XP_011526547.1:p.Val929Glu
XM_011528246.1:c.2489T>A	XP_011526548.1:p.Val830Glu
XM_011528247.1:c.2489T>A	XP_011526549.1:p.Val830Glu
XM_011528248.1:c.2786T>A	XP_011526550.1:p.Val929Glu
XM_011528249.1:c.1460T>A	XP_011526551.1:p.Val487Glu
XM_011528251.1:c.1043T>A	XP_011526553.1:p.Val348Glu
XM_011528246.3:c.2489T>A	XP_011526548.1:p.Val830Glu
XM_011528249.2:c.1460T>A	XP_011526551.1:p.Val487Glu
XR_001753750.1:n.2943T>A
XR_001753751.1:n.2943T>A
XR_002958353.1:n.3869T>A
NM_003331.5:c.2786T>A MANE Select	NP_003322.3:p.Val929Glu
NM_001385197.1:c.2786T>A	NP_001372126.1:p.Val929Glu
NM_001385198.1:c.2786T>A	NP_001372127.1:p.Val929Glu
NM_001385199.1:c.2600T>A	NP_001372128.1:p.Val867Glu
NM_001385200.1:c.2783T>A	NP_001372129.1:p.Val928Glu
NM_001385201.1:c.2588T>A	NP_001372130.1:p.Val863Glu
NM_001385202.1:c.2702T>A	NP_001372131.1:p.Val901Glu
NM_001385203.1:c.2867T>A	NP_001372132.1:p.Val956Glu
NM_001385204.1:c.2996T>A	NP_001372133.1:p.Val999Glu
NM_001385205.1:c.2696T>A	NP_001372134.1:p.Val899Glu
NM_001385206.1:c.2660T>A	NP_001372135.1:p.Val887Glu
NM_001385207.1:c.2768T>A	NP_001372136.1:p.Val923Glu