Canonical Allele Identifier: CA403987809

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464752G>T (hg19) ; chr19:g.10354076G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354076G>T , CM000681.2:g.10354076G>T	GRCh38
NC_000019.9:g.10464752G>T , CM000681.1:g.10464752G>T	GRCh37
NC_000019.8:g.10325752G>T	NCBI36
NG_007872.1:g.31497C>A , LRG_121:g.31497C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1223C>A	ENSP00000514307.1:n.*1223C>A
ENST00000525976.6:c.2874C>A	ENSP00000434831.2:p.His958Gln
ENST00000527481.3:c.2874C>A	ENSP00000466340.2:p.His958Gln
ENST00000529370.6:n.4250C>A
ENST00000529739.2:n.3288C>A
ENST00000530829.2:c.*2425C>A	ENSP00000436826.2:n.*2425C>A
ENST00000531836.6:c.2874C>A	ENSP00000436175.2:p.His958Gln
ENST00000533334.2:c.*916C>A	ENSP00000432320.2:n.*916C>A
ENST00000534228.2:n.4333C>A
ENST00000699354.1:n.976C>A
ENST00000699355.1:c.*1979C>A	ENSP00000514328.1:n.*1979C>A
ENST00000699356.1:n.3288C>A
ENST00000699357.1:n.4333C>A
ENST00000699358.1:c.2874C>A	ENSP00000514329.1:p.His958Gln
ENST00000699359.1:c.80C>A
ENST00000699360.1:c.2874C>A	ENSP00000514331.1:p.His958Gln
ENST00000699368.1:c.78C>A	ENSP00000514335.1:p.His26Gln
ENST00000525621.6:c.2874C>A MANE Select	ENSP00000431885.1:p.His958Gln
ENST00000264818.10:c.2874C>A	ENSP00000264818.6:p.His958Gln
ENST00000524462.5:c.2319C>A	ENSP00000433203.1:p.His773Gln
ENST00000525621.5:c.2874C>A	ENSP00000431885.1:p.His958Gln
ENST00000527481.2:c.170C>A
ENST00000529412.1:n.546C>A
ENST00000529739.1:c.-453C>A	ENSP00000436155.1:n.-453C>A
ENST00000530560.5:c.303C>A	ENSP00000465291.1:p.His101Gln
ENST00000592137.1:n.28C>A
NM_003331.4:c.2874C>A , LRG_121t1:c.2874C>A	NP_003322.3:p.His958Gln
XM_011528245.1:c.2874C>A	XP_011526547.1:p.His958Gln
XM_011528246.1:c.2577C>A	XP_011526548.1:p.His859Gln
XM_011528247.1:c.2577C>A	XP_011526549.1:p.His859Gln
XM_011528248.1:c.2874C>A	XP_011526550.1:p.His958Gln
XM_011528249.1:c.1548C>A	XP_011526551.1:p.His516Gln
XM_011528251.1:c.1131C>A	XP_011526553.1:p.His377Gln
XM_011528246.3:c.2577C>A	XP_011526548.1:p.His859Gln
XM_011528249.2:c.1548C>A	XP_011526551.1:p.His516Gln
XR_001753750.1:n.3031C>A
XR_001753751.1:n.3031C>A
XR_002958353.1:n.3957C>A
NM_003331.5:c.2874C>A MANE Select	NP_003322.3:p.His958Gln
NM_001385197.1:c.2874C>A	NP_001372126.1:p.His958Gln
NM_001385198.1:c.2874C>A	NP_001372127.1:p.His958Gln
NM_001385199.1:c.2688C>A	NP_001372128.1:p.His896Gln
NM_001385200.1:c.2871C>A	NP_001372129.1:p.His957Gln
NM_001385201.1:c.2676C>A	NP_001372130.1:p.His892Gln
NM_001385202.1:c.2790C>A	NP_001372131.1:p.His930Gln
NM_001385203.1:c.2955C>A	NP_001372132.1:p.His985Gln
NM_001385204.1:c.3084C>A	NP_001372133.1:p.His1028Gln
NM_001385205.1:c.2784C>A	NP_001372134.1:p.His928Gln
NM_001385206.1:c.2748C>A	NP_001372135.1:p.His916Gln
NM_001385207.1:c.2856C>A	NP_001372136.1:p.His952Gln