Canonical Allele Identifier: CA403987580

Gene: TYK2

Linked Data

• dbSNP Id: rs1301255042
• gnomAD v2: 19-10464721-G-C
• gnomAD v4: 19-10354045-G-C
• MyVariant Identifiers: chr19:g.10464721G>C (hg19) ; chr19:g.10354045G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354045G>C , CM000681.2:g.10354045G>C	GRCh38
NC_000019.9:g.10464721G>C , CM000681.1:g.10464721G>C	GRCh37
NC_000019.8:g.10325721G>C	NCBI36
NG_007872.1:g.31528C>G , LRG_121:g.31528C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1254C>G	ENSP00000514307.1:n.*1254C>G
ENST00000525976.6:c.2905C>G	ENSP00000434831.2:p.Gln969Glu
ENST00000527481.3:c.2905C>G	ENSP00000466340.2:p.Gln969Glu
ENST00000529370.6:n.4281C>G
ENST00000529739.2:n.3319C>G
ENST00000530829.2:c.*2456C>G	ENSP00000436826.2:n.*2456C>G
ENST00000531836.6:c.2905C>G	ENSP00000436175.2:p.Gln969Glu
ENST00000533334.2:c.*947C>G	ENSP00000432320.2:n.*947C>G
ENST00000534228.2:n.4364C>G
ENST00000699354.1:n.1007C>G
ENST00000699355.1:c.*2010C>G	ENSP00000514328.1:n.*2010C>G
ENST00000699356.1:n.3319C>G
ENST00000699357.1:n.4364C>G
ENST00000699358.1:c.2905C>G	ENSP00000514329.1:p.Gln969Glu
ENST00000699359.1:c.111C>G
ENST00000699360.1:c.2905C>G	ENSP00000514331.1:p.Gln969Glu
ENST00000699368.1:c.109C>G	ENSP00000514335.1:p.Gln37Glu
ENST00000525621.6:c.2905C>G MANE Select	ENSP00000431885.1:p.Gln969Glu
ENST00000264818.10:c.2905C>G	ENSP00000264818.6:p.Gln969Glu
ENST00000524462.5:c.2350C>G	ENSP00000433203.1:p.Gln784Glu
ENST00000525621.5:c.2905C>G	ENSP00000431885.1:p.Gln969Glu
ENST00000527481.2:c.201C>G
ENST00000529412.1:n.577C>G
ENST00000529739.1:c.-422C>G	ENSP00000436155.1:n.-422C>G
ENST00000530560.5:c.334C>G	ENSP00000465291.1:p.Gln112Glu
ENST00000592137.1:n.59C>G
NM_003331.4:c.2905C>G , LRG_121t1:c.2905C>G	NP_003322.3:p.Gln969Glu
XM_011528245.1:c.2905C>G	XP_011526547.1:p.Gln969Glu
XM_011528246.1:c.2608C>G	XP_011526548.1:p.Gln870Glu
XM_011528247.1:c.2608C>G	XP_011526549.1:p.Gln870Glu
XM_011528248.1:c.2905C>G	XP_011526550.1:p.Gln969Glu
XM_011528249.1:c.1579C>G	XP_011526551.1:p.Gln527Glu
XM_011528251.1:c.1162C>G	XP_011526553.1:p.Gln388Glu
XM_011528246.3:c.2608C>G	XP_011526548.1:p.Gln870Glu
XM_011528249.2:c.1579C>G	XP_011526551.1:p.Gln527Glu
XR_001753750.1:n.3062C>G
XR_001753751.1:n.3062C>G
XR_002958353.1:n.3988C>G
NM_003331.5:c.2905C>G MANE Select	NP_003322.3:p.Gln969Glu
NM_001385197.1:c.2905C>G	NP_001372126.1:p.Gln969Glu
NM_001385198.1:c.2905C>G	NP_001372127.1:p.Gln969Glu
NM_001385199.1:c.2719C>G	NP_001372128.1:p.Gln907Glu
NM_001385200.1:c.2902C>G	NP_001372129.1:p.Gln968Glu
NM_001385201.1:c.2707C>G	NP_001372130.1:p.Gln903Glu
NM_001385202.1:c.2821C>G	NP_001372131.1:p.Gln941Glu
NM_001385203.1:c.2986C>G	NP_001372132.1:p.Gln996Glu
NM_001385204.1:c.3115C>G	NP_001372133.1:p.Gln1039Glu
NM_001385205.1:c.2815C>G	NP_001372134.1:p.Gln939Glu
NM_001385206.1:c.2779C>G	NP_001372135.1:p.Gln927Glu
NM_001385207.1:c.2887C>G	NP_001372136.1:p.Gln963Glu