Canonical Allele Identifier: CA403989037

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464879T>C (hg19) ; chr19:g.10354203T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354203T>C , CM000681.2:g.10354203T>C	GRCh38
NC_000019.9:g.10464879T>C , CM000681.1:g.10464879T>C	GRCh37
NC_000019.8:g.10325879T>C	NCBI36
NG_007872.1:g.31370A>G , LRG_121:g.31370A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1096A>G	ENSP00000514307.1:n.*1096A>G
ENST00000525976.6:c.2747A>G	ENSP00000434831.2:p.Tyr916Cys
ENST00000527481.3:c.2747A>G	ENSP00000466340.2:p.Tyr916Cys
ENST00000529370.6:n.4123A>G
ENST00000529739.2:n.3161A>G
ENST00000530829.2:c.*2298A>G	ENSP00000436826.2:n.*2298A>G
ENST00000531836.6:c.2747A>G	ENSP00000436175.2:p.Tyr916Cys
ENST00000533334.2:c.*789A>G	ENSP00000432320.2:n.*789A>G
ENST00000534228.2:n.4206A>G
ENST00000699354.1:n.849A>G
ENST00000699355.1:c.*1852A>G	ENSP00000514328.1:n.*1852A>G
ENST00000699356.1:n.3161A>G
ENST00000699357.1:n.4206A>G
ENST00000699358.1:c.2747A>G	ENSP00000514329.1:p.Tyr916Cys
ENST00000699360.1:c.2747A>G	ENSP00000514331.1:p.Tyr916Cys
ENST00000525621.6:c.2747A>G MANE Select	ENSP00000431885.1:p.Tyr916Cys
ENST00000264818.10:c.2747A>G	ENSP00000264818.6:p.Tyr916Cys
ENST00000524462.5:c.2192A>G	ENSP00000433203.1:p.Tyr731Cys
ENST00000525621.5:c.2747A>G	ENSP00000431885.1:p.Tyr916Cys
ENST00000527481.2:c.43A>G
ENST00000529412.1:n.419A>G
ENST00000530560.5:c.176A>G	ENSP00000465291.1:p.Tyr59Cys
NM_003331.4:c.2747A>G , LRG_121t1:c.2747A>G	NP_003322.3:p.Tyr916Cys
XM_011528245.1:c.2747A>G	XP_011526547.1:p.Tyr916Cys
XM_011528246.1:c.2450A>G	XP_011526548.1:p.Tyr817Cys
XM_011528247.1:c.2450A>G	XP_011526549.1:p.Tyr817Cys
XM_011528248.1:c.2747A>G	XP_011526550.1:p.Tyr916Cys
XM_011528249.1:c.1421A>G	XP_011526551.1:p.Tyr474Cys
XM_011528251.1:c.1004A>G	XP_011526553.1:p.Tyr335Cys
XM_011528246.3:c.2450A>G	XP_011526548.1:p.Tyr817Cys
XM_011528249.2:c.1421A>G	XP_011526551.1:p.Tyr474Cys
XR_001753750.1:n.2904A>G
XR_001753751.1:n.2904A>G
XR_002958353.1:n.3830A>G
NM_003331.5:c.2747A>G MANE Select	NP_003322.3:p.Tyr916Cys
NM_001385197.1:c.2747A>G	NP_001372126.1:p.Tyr916Cys
NM_001385198.1:c.2747A>G	NP_001372127.1:p.Tyr916Cys
NM_001385199.1:c.2561A>G	NP_001372128.1:p.Tyr854Cys
NM_001385200.1:c.2744A>G	NP_001372129.1:p.Tyr915Cys
NM_001385201.1:c.2549A>G	NP_001372130.1:p.Tyr850Cys
NM_001385202.1:c.2663A>G	NP_001372131.1:p.Tyr888Cys
NM_001385203.1:c.2828A>G	NP_001372132.1:p.Tyr943Cys
NM_001385204.1:c.2957A>G	NP_001372133.1:p.Tyr986Cys
NM_001385205.1:c.2657A>G	NP_001372134.1:p.Tyr886Cys
NM_001385206.1:c.2621A>G	NP_001372135.1:p.Tyr874Cys
NM_001385207.1:c.2729A>G	NP_001372136.1:p.Tyr910Cys