Canonical Allele Identifier: CA403989395

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464911C>T (hg19) ; chr19:g.10354235C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354235C>T , CM000681.2:g.10354235C>T	GRCh38
NC_000019.9:g.10464911C>T , CM000681.1:g.10464911C>T	GRCh37
NC_000019.8:g.10325911C>T	NCBI36
NG_007872.1:g.31338G>A , LRG_121:g.31338G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1065-1G>A	ENSP00000514307.1:n.*1065-1G>A
ENST00000525976.6:c.2716-1G>A	ENSP00000434831.2:n.2716-1G>A
ENST00000527481.3:c.2716-1G>A	ENSP00000466340.2:n.2716-1G>A
ENST00000529370.6:n.4092-1G>A
ENST00000529739.2:n.3130-1G>A
ENST00000530829.2:c.*2267-1G>A	ENSP00000436826.2:n.*2267-1G>A
ENST00000531836.6:c.2716-1G>A	ENSP00000436175.2:n.2716-1G>A
ENST00000533334.2:c.*758-1G>A	ENSP00000432320.2:n.*758-1G>A
ENST00000534228.2:n.4175-1G>A
ENST00000699354.1:n.818-1G>A
ENST00000699355.1:c.*1821-1G>A	ENSP00000514328.1:n.*1821-1G>A
ENST00000699356.1:n.3130-1G>A
ENST00000699357.1:n.4175-1G>A
ENST00000699358.1:c.2716-1G>A	ENSP00000514329.1:n.2716-1G>A
ENST00000699360.1:c.2716-1G>A	ENSP00000514331.1:n.2716-1G>A
ENST00000525621.6:c.2716-1G>A MANE Select	ENSP00000431885.1:n.2716-1G>A
ENST00000264818.10:c.2716-1G>A	ENSP00000264818.6:n.2716-1G>A
ENST00000524462.5:c.2161-1G>A	ENSP00000433203.1:n.2161-1G>A
ENST00000525621.5:c.2716-1G>A	ENSP00000431885.1:n.2716-1G>A
ENST00000527481.2:c.12-1G>A
ENST00000529412.1:n.388-1G>A
ENST00000530560.5:c.145-1G>A	ENSP00000465291.1:n.145-1G>A
NM_003331.4:c.2716-1G>A , LRG_121t1:c.2716-1G>A	NP_003322.3:n.2716-1G>A
XM_011528245.1:c.2716-1G>A	XP_011526547.1:n.2716-1G>A
XM_011528246.1:c.2419-1G>A	XP_011526548.1:n.2419-1G>A
XM_011528247.1:c.2419-1G>A	XP_011526549.1:n.2419-1G>A
XM_011528248.1:c.2716-1G>A	XP_011526550.1:n.2716-1G>A
XM_011528249.1:c.1390-1G>A	XP_011526551.1:n.1390-1G>A
XM_011528251.1:c.973-1G>A	XP_011526553.1:n.973-1G>A
XM_011528246.3:c.2419-1G>A	XP_011526548.1:n.2419-1G>A
XM_011528249.2:c.1390-1G>A	XP_011526551.1:n.1390-1G>A
XR_001753750.1:n.2873-1G>A
XR_001753751.1:n.2873-1G>A
XR_002958353.1:n.3799-1G>A
NM_003331.5:c.2716-1G>A MANE Select	NP_003322.3:n.2716-1G>A
NM_001385197.1:c.2716-1G>A	NP_001372126.1:n.2716-1G>A
NM_001385198.1:c.2716-1G>A	NP_001372127.1:n.2716-1G>A
NM_001385199.1:c.2530-1G>A	NP_001372128.1:n.2530-1G>A
NM_001385200.1:c.2713-1G>A	NP_001372129.1:n.2713-1G>A
NM_001385201.1:c.2518-1G>A	NP_001372130.1:n.2518-1G>A
NM_001385202.1:c.2632-1G>A	NP_001372131.1:n.2632-1G>A
NM_001385203.1:c.2797-1G>A	NP_001372132.1:n.2797-1G>A
NM_001385204.1:c.2926-1G>A	NP_001372133.1:n.2926-1G>A
NM_001385205.1:c.2626-1G>A	NP_001372134.1:n.2626-1G>A
NM_001385206.1:c.2590-1G>A	NP_001372135.1:n.2590-1G>A
NM_001385207.1:c.2698-1G>A	NP_001372136.1:n.2698-1G>A