Canonical Allele Identifier: CA403987701

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464741T>A (hg19) ; chr19:g.10354065T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354065T>A , CM000681.2:g.10354065T>A	GRCh38
NC_000019.9:g.10464741T>A , CM000681.1:g.10464741T>A	GRCh37
NC_000019.8:g.10325741T>A	NCBI36
NG_007872.1:g.31508A>T , LRG_121:g.31508A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1234A>T	ENSP00000514307.1:n.*1234A>T
ENST00000525976.6:c.2885A>T	ENSP00000434831.2:p.Tyr962Phe
ENST00000527481.3:c.2885A>T	ENSP00000466340.2:p.Tyr962Phe
ENST00000529370.6:n.4261A>T
ENST00000529739.2:n.3299A>T
ENST00000530829.2:c.*2436A>T	ENSP00000436826.2:n.*2436A>T
ENST00000531836.6:c.2885A>T	ENSP00000436175.2:p.Tyr962Phe
ENST00000533334.2:c.*927A>T	ENSP00000432320.2:n.*927A>T
ENST00000534228.2:n.4344A>T
ENST00000699354.1:n.987A>T
ENST00000699355.1:c.*1990A>T	ENSP00000514328.1:n.*1990A>T
ENST00000699356.1:n.3299A>T
ENST00000699357.1:n.4344A>T
ENST00000699358.1:c.2885A>T	ENSP00000514329.1:p.Tyr962Phe
ENST00000699359.1:c.91A>T
ENST00000699360.1:c.2885A>T	ENSP00000514331.1:p.Tyr962Phe
ENST00000699368.1:c.89A>T	ENSP00000514335.1:p.Tyr30Phe
ENST00000525621.6:c.2885A>T MANE Select	ENSP00000431885.1:p.Tyr962Phe
ENST00000264818.10:c.2885A>T	ENSP00000264818.6:p.Tyr962Phe
ENST00000524462.5:c.2330A>T	ENSP00000433203.1:p.Tyr777Phe
ENST00000525621.5:c.2885A>T	ENSP00000431885.1:p.Tyr962Phe
ENST00000527481.2:c.181A>T
ENST00000529412.1:n.557A>T
ENST00000529739.1:c.-442A>T	ENSP00000436155.1:n.-442A>T
ENST00000530560.5:c.314A>T	ENSP00000465291.1:p.Tyr105Phe
ENST00000592137.1:n.39A>T
NM_003331.4:c.2885A>T , LRG_121t1:c.2885A>T	NP_003322.3:p.Tyr962Phe
XM_011528245.1:c.2885A>T	XP_011526547.1:p.Tyr962Phe
XM_011528246.1:c.2588A>T	XP_011526548.1:p.Tyr863Phe
XM_011528247.1:c.2588A>T	XP_011526549.1:p.Tyr863Phe
XM_011528248.1:c.2885A>T	XP_011526550.1:p.Tyr962Phe
XM_011528249.1:c.1559A>T	XP_011526551.1:p.Tyr520Phe
XM_011528251.1:c.1142A>T	XP_011526553.1:p.Tyr381Phe
XM_011528246.3:c.2588A>T	XP_011526548.1:p.Tyr863Phe
XM_011528249.2:c.1559A>T	XP_011526551.1:p.Tyr520Phe
XR_001753750.1:n.3042A>T
XR_001753751.1:n.3042A>T
XR_002958353.1:n.3968A>T
NM_003331.5:c.2885A>T MANE Select	NP_003322.3:p.Tyr962Phe
NM_001385197.1:c.2885A>T	NP_001372126.1:p.Tyr962Phe
NM_001385198.1:c.2885A>T	NP_001372127.1:p.Tyr962Phe
NM_001385199.1:c.2699A>T	NP_001372128.1:p.Tyr900Phe
NM_001385200.1:c.2882A>T	NP_001372129.1:p.Tyr961Phe
NM_001385201.1:c.2687A>T	NP_001372130.1:p.Tyr896Phe
NM_001385202.1:c.2801A>T	NP_001372131.1:p.Tyr934Phe
NM_001385203.1:c.2966A>T	NP_001372132.1:p.Tyr989Phe
NM_001385204.1:c.3095A>T	NP_001372133.1:p.Tyr1032Phe
NM_001385205.1:c.2795A>T	NP_001372134.1:p.Tyr932Phe
NM_001385206.1:c.2759A>T	NP_001372135.1:p.Tyr920Phe
NM_001385207.1:c.2867A>T	NP_001372136.1:p.Tyr956Phe