Canonical Allele Identifier: CA403987571

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464720T>G (hg19) ; chr19:g.10354044T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354044T>G , CM000681.2:g.10354044T>G	GRCh38
NC_000019.9:g.10464720T>G , CM000681.1:g.10464720T>G	GRCh37
NC_000019.8:g.10325720T>G	NCBI36
NG_007872.1:g.31529A>C , LRG_121:g.31529A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1255A>C	ENSP00000514307.1:n.*1255A>C
ENST00000525976.6:c.2906A>C	ENSP00000434831.2:p.Gln969Pro
ENST00000527481.3:c.2906A>C	ENSP00000466340.2:p.Gln969Pro
ENST00000529370.6:n.4282A>C
ENST00000529739.2:n.3320A>C
ENST00000530829.2:c.*2457A>C	ENSP00000436826.2:n.*2457A>C
ENST00000531836.6:c.2906A>C	ENSP00000436175.2:p.Gln969Pro
ENST00000533334.2:c.*948A>C	ENSP00000432320.2:n.*948A>C
ENST00000534228.2:n.4365A>C
ENST00000699354.1:n.1008A>C
ENST00000699355.1:c.*2011A>C	ENSP00000514328.1:n.*2011A>C
ENST00000699356.1:n.3320A>C
ENST00000699357.1:n.4365A>C
ENST00000699358.1:c.2906A>C	ENSP00000514329.1:p.Gln969Pro
ENST00000699359.1:c.112A>C
ENST00000699360.1:c.2906A>C	ENSP00000514331.1:p.Gln969Pro
ENST00000699368.1:c.110A>C	ENSP00000514335.1:p.Gln37Pro
ENST00000525621.6:c.2906A>C MANE Select	ENSP00000431885.1:p.Gln969Pro
ENST00000264818.10:c.2906A>C	ENSP00000264818.6:p.Gln969Pro
ENST00000524462.5:c.2351A>C	ENSP00000433203.1:p.Gln784Pro
ENST00000525621.5:c.2906A>C	ENSP00000431885.1:p.Gln969Pro
ENST00000527481.2:c.202A>C
ENST00000529412.1:n.578A>C
ENST00000529739.1:c.-421A>C	ENSP00000436155.1:n.-421A>C
ENST00000530560.5:c.335A>C	ENSP00000465291.1:p.Gln112Pro
ENST00000592137.1:n.60A>C
NM_003331.4:c.2906A>C , LRG_121t1:c.2906A>C	NP_003322.3:p.Gln969Pro
XM_011528245.1:c.2906A>C	XP_011526547.1:p.Gln969Pro
XM_011528246.1:c.2609A>C	XP_011526548.1:p.Gln870Pro
XM_011528247.1:c.2609A>C	XP_011526549.1:p.Gln870Pro
XM_011528248.1:c.2906A>C	XP_011526550.1:p.Gln969Pro
XM_011528249.1:c.1580A>C	XP_011526551.1:p.Gln527Pro
XM_011528251.1:c.1163A>C	XP_011526553.1:p.Gln388Pro
XM_011528246.3:c.2609A>C	XP_011526548.1:p.Gln870Pro
XM_011528249.2:c.1580A>C	XP_011526551.1:p.Gln527Pro
XR_001753750.1:n.3063A>C
XR_001753751.1:n.3063A>C
XR_002958353.1:n.3989A>C
NM_003331.5:c.2906A>C MANE Select	NP_003322.3:p.Gln969Pro
NM_001385197.1:c.2906A>C	NP_001372126.1:p.Gln969Pro
NM_001385198.1:c.2906A>C	NP_001372127.1:p.Gln969Pro
NM_001385199.1:c.2720A>C	NP_001372128.1:p.Gln907Pro
NM_001385200.1:c.2903A>C	NP_001372129.1:p.Gln968Pro
NM_001385201.1:c.2708A>C	NP_001372130.1:p.Gln903Pro
NM_001385202.1:c.2822A>C	NP_001372131.1:p.Gln941Pro
NM_001385203.1:c.2987A>C	NP_001372132.1:p.Gln996Pro
NM_001385204.1:c.3116A>C	NP_001372133.1:p.Gln1039Pro
NM_001385205.1:c.2816A>C	NP_001372134.1:p.Gln939Pro
NM_001385206.1:c.2780A>C	NP_001372135.1:p.Gln927Pro
NM_001385207.1:c.2888A>C	NP_001372136.1:p.Gln963Pro