Canonical Allele Identifier: CA403988912

Gene: TYK2

Linked Data

• dbSNP Id: rs2040964074
• MyVariant Identifiers: chr19:g.10464866G>C (hg19) ; chr19:g.10354190G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354190G>C , CM000681.2:g.10354190G>C	GRCh38
NC_000019.9:g.10464866G>C , CM000681.1:g.10464866G>C	GRCh37
NC_000019.8:g.10325866G>C	NCBI36
NG_007872.1:g.31383C>G , LRG_121:g.31383C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1109C>G	ENSP00000514307.1:n.*1109C>G
ENST00000525976.6:c.2760C>G	ENSP00000434831.2:p.Asn920Lys
ENST00000527481.3:c.2760C>G	ENSP00000466340.2:p.Asn920Lys
ENST00000529370.6:n.4136C>G
ENST00000529739.2:n.3174C>G
ENST00000530829.2:c.*2311C>G	ENSP00000436826.2:n.*2311C>G
ENST00000531836.6:c.2760C>G	ENSP00000436175.2:p.Asn920Lys
ENST00000533334.2:c.*802C>G	ENSP00000432320.2:n.*802C>G
ENST00000534228.2:n.4219C>G
ENST00000699354.1:n.862C>G
ENST00000699355.1:c.*1865C>G	ENSP00000514328.1:n.*1865C>G
ENST00000699356.1:n.3174C>G
ENST00000699357.1:n.4219C>G
ENST00000699358.1:c.2760C>G	ENSP00000514329.1:p.Asn920Lys
ENST00000699360.1:c.2760C>G	ENSP00000514331.1:p.Asn920Lys
ENST00000525621.6:c.2760C>G MANE Select	ENSP00000431885.1:p.Asn920Lys
ENST00000264818.10:c.2760C>G	ENSP00000264818.6:p.Asn920Lys
ENST00000524462.5:c.2205C>G	ENSP00000433203.1:p.Asn735Lys
ENST00000525621.5:c.2760C>G	ENSP00000431885.1:p.Asn920Lys
ENST00000527481.2:c.56C>G
ENST00000529412.1:n.432C>G
ENST00000530560.5:c.189C>G	ENSP00000465291.1:p.Asn63Lys
NM_003331.4:c.2760C>G , LRG_121t1:c.2760C>G	NP_003322.3:p.Asn920Lys
XM_011528245.1:c.2760C>G	XP_011526547.1:p.Asn920Lys
XM_011528246.1:c.2463C>G	XP_011526548.1:p.Asn821Lys
XM_011528247.1:c.2463C>G	XP_011526549.1:p.Asn821Lys
XM_011528248.1:c.2760C>G	XP_011526550.1:p.Asn920Lys
XM_011528249.1:c.1434C>G	XP_011526551.1:p.Asn478Lys
XM_011528251.1:c.1017C>G	XP_011526553.1:p.Asn339Lys
XM_011528246.3:c.2463C>G	XP_011526548.1:p.Asn821Lys
XM_011528249.2:c.1434C>G	XP_011526551.1:p.Asn478Lys
XR_001753750.1:n.2917C>G
XR_001753751.1:n.2917C>G
XR_002958353.1:n.3843C>G
NM_003331.5:c.2760C>G MANE Select	NP_003322.3:p.Asn920Lys
NM_001385197.1:c.2760C>G	NP_001372126.1:p.Asn920Lys
NM_001385198.1:c.2760C>G	NP_001372127.1:p.Asn920Lys
NM_001385199.1:c.2574C>G	NP_001372128.1:p.Asn858Lys
NM_001385200.1:c.2757C>G	NP_001372129.1:p.Asn919Lys
NM_001385201.1:c.2562C>G	NP_001372130.1:p.Asn854Lys
NM_001385202.1:c.2676C>G	NP_001372131.1:p.Asn892Lys
NM_001385203.1:c.2841C>G	NP_001372132.1:p.Asn947Lys
NM_001385204.1:c.2970C>G	NP_001372133.1:p.Asn990Lys
NM_001385205.1:c.2670C>G	NP_001372134.1:p.Asn890Lys
NM_001385206.1:c.2634C>G	NP_001372135.1:p.Asn878Lys
NM_001385207.1:c.2742C>G	NP_001372136.1:p.Asn914Lys