Canonical Allele Identifier: CA403982956

Gene: TYK2

Linked Data

• gnomAD v4: 19-10352449-G-C
• MyVariant Identifiers: chr19:g.10463125G>C (hg19) ; chr19:g.10352449G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352449G>C , CM000681.2:g.10352449G>C	GRCh38
NC_000019.9:g.10463125G>C , CM000681.1:g.10463125G>C	GRCh37
NC_000019.8:g.10324125G>C	NCBI36
NG_007872.1:g.33124C>G , LRG_121:g.33124C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.*1652C>G	ENSP00000514307.1:n.*1652C>G
ENST00000525976.6:c.3303C>G	ENSP00000434831.2:p.Ser1101Arg
ENST00000527481.3:c.*73C>G	ENSP00000466340.2:n.*73C>G
ENST00000529370.6:n.4679C>G
ENST00000529739.2:n.4112C>G
ENST00000530829.2:c.*2854C>G	ENSP00000436826.2:n.*2854C>G
ENST00000531836.6:c.3303C>G	ENSP00000436175.2:p.Ser1101Arg
ENST00000533334.2:c.*1242+477C>G	ENSP00000432320.2:n.*1242+477C>G
ENST00000534228.2:n.5054+477C>G
ENST00000699354.1:n.1405C>G
ENST00000699355.1:c.*2803C>G	ENSP00000514328.1:n.*2803C>G
ENST00000699356.1:n.4112C>G
ENST00000699357.1:n.5157C>G
ENST00000699358.1:c.3200+477C>G	ENSP00000514329.1:n.3200+477C>G
ENST00000699359.1:c.477C>G
ENST00000699360.1:c.3261C>G	ENSP00000514331.1:p.Ser1087Arg
ENST00000699361.1:n.337C>G
ENST00000699362.1:c.199C>G	ENSP00000514332.1:n.199C>G
ENST00000699363.1:c.199C>G	ENSP00000514333.1:n.199C>G
ENST00000699364.1:n.303C>G
ENST00000699365.1:c.372C>G	ENSP00000514334.1:p.Ser124Arg
ENST00000699366.1:n.111+1365C>G
ENST00000699367.1:n.112-1287C>G
ENST00000699368.1:c.790C>G	ENSP00000514335.1:n.790C>G
ENST00000525621.6:c.3303C>G MANE Select	ENSP00000431885.1:p.Ser1101Arg
ENST00000264818.10:c.3303C>G	ENSP00000264818.6:p.Ser1101Arg
ENST00000524462.5:c.2748C>G	ENSP00000433203.1:p.Ser916Arg
ENST00000525621.5:c.3303C>G	ENSP00000431885.1:p.Ser1101Arg
ENST00000525976.5:c.44C>G
ENST00000527481.2:c.480C>G
ENST00000529422.1:n.116+573C>G
ENST00000529739.1:c.372C>G	ENSP00000436155.1:p.Ser124Arg
ENST00000530220.1:n.331+477C>G
ENST00000530560.5:c.338-1481C>G	ENSP00000465291.1:n.338-1481C>G
ENST00000592137.1:n.457C>G
NM_003331.4:c.3303C>G , LRG_121t1:c.3303C>G	NP_003322.3:p.Ser1101Arg
XM_011528245.1:c.3303C>G	XP_011526547.1:p.Ser1101Arg
XM_011528246.1:c.3006C>G	XP_011526548.1:p.Ser1002Arg
XM_011528247.1:c.3006C>G	XP_011526549.1:p.Ser1002Arg
XM_011528248.1:c.3200+477C>G	XP_011526550.1:n.3200+477C>G
XM_011528249.1:c.1977C>G	XP_011526551.1:p.Ser659Arg
XM_011528251.1:c.1560C>G	XP_011526553.1:p.Ser520Arg
XM_011528246.3:c.3006C>G	XP_011526548.1:p.Ser1002Arg
XM_011528249.2:c.1977C>G	XP_011526551.1:p.Ser659Arg
XR_001753750.1:n.3357+477C>G
XR_001753751.1:n.3855C>G
XR_002958353.1:n.4781C>G
NM_003331.5:c.3303C>G MANE Select	NP_003322.3:p.Ser1101Arg
NM_001385197.1:c.3303C>G	NP_001372126.1:p.Ser1101Arg
NM_001385198.1:c.3168+509C>G	NP_001372127.1:n.3168+509C>G
NM_001385199.1:c.3117C>G	NP_001372128.1:p.Ser1039Arg
NM_001385200.1:c.3300C>G	NP_001372129.1:p.Ser1100Arg
NM_001385201.1:c.3105C>G	NP_001372130.1:p.Ser1035Arg
NM_001385202.1:c.3219C>G	NP_001372131.1:p.Ser1073Arg
NM_001385203.1:c.3384C>G	NP_001372132.1:p.Ser1128Arg
NM_001385204.1:c.3513C>G	NP_001372133.1:p.Ser1171Arg
NM_001385205.1:c.3213C>G	NP_001372134.1:p.Ser1071Arg
NM_001385206.1:c.3177C>G	NP_001372135.1:p.Ser1059Arg
NM_001385207.1:c.3285C>G	NP_001372136.1:p.Ser1095Arg