Canonical Allele Identifier: CA403996347

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10468687G>T (hg19) ; chr19:g.10358011G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10358011G>T , CM000681.2:g.10358011G>T	GRCh38
NC_000019.9:g.10468687G>T , CM000681.1:g.10468687G>T	GRCh37
NC_000019.8:g.10329687G>T	NCBI36
NG_007872.1:g.27562C>A , LRG_121:g.27562C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.*652C>A	ENSP00000514307.1:n.*652C>A
ENST00000525976.6:c.2303C>A	ENSP00000434831.2:p.Ser768Tyr
ENST00000527481.3:c.2303C>A	ENSP00000466340.2:p.Ser768Tyr
ENST00000529370.6:n.2634C>A
ENST00000529739.2:n.2717C>A
ENST00000530829.2:c.*1854C>A	ENSP00000436826.2:n.*1854C>A
ENST00000531836.6:c.2303C>A	ENSP00000436175.2:p.Ser768Tyr
ENST00000533334.2:c.*345C>A	ENSP00000432320.2:n.*345C>A
ENST00000534228.2:n.2717C>A
ENST00000699354.1:n.405C>A
ENST00000699355.1:c.*363C>A	ENSP00000514328.1:n.*363C>A
ENST00000699356.1:n.2717C>A
ENST00000699357.1:n.2717C>A
ENST00000699358.1:c.2303C>A	ENSP00000514329.1:p.Ser768Tyr
ENST00000699360.1:c.2303C>A	ENSP00000514331.1:p.Ser768Tyr
ENST00000525621.6:c.2303C>A MANE Select	ENSP00000431885.1:p.Ser768Tyr
ENST00000264818.10:c.2303C>A	ENSP00000264818.6:p.Ser768Tyr
ENST00000524462.5:c.1748C>A	ENSP00000433203.1:p.Ser583Tyr
ENST00000525621.5:c.2303C>A	ENSP00000431885.1:p.Ser768Tyr
ENST00000529370.5:c.2303C>A	ENSP00000432728.1:p.Ser768Tyr
ENST00000533334.1:c.592C>A
NM_003331.4:c.2303C>A , LRG_121t1:c.2303C>A	NP_003322.3:p.Ser768Tyr
XM_011528245.1:c.2303C>A	XP_011526547.1:p.Ser768Tyr
XM_011528246.1:c.2006C>A	XP_011526548.1:p.Ser669Tyr
XM_011528247.1:c.2006C>A	XP_011526549.1:p.Ser669Tyr
XM_011528248.1:c.2303C>A	XP_011526550.1:p.Ser768Tyr
XM_011528249.1:c.977C>A	XP_011526551.1:p.Ser326Tyr
XM_011528251.1:c.560C>A	XP_011526553.1:p.Ser187Tyr
XM_011528246.3:c.2006C>A	XP_011526548.1:p.Ser669Tyr
XM_011528249.2:c.977C>A	XP_011526551.1:p.Ser326Tyr
XR_001753750.1:n.2460C>A
XR_001753751.1:n.2460C>A
XR_001753752.1:n.2572C>A
XR_002958353.1:n.2341C>A
NM_003331.5:c.2303C>A MANE Select	NP_003322.3:p.Ser768Tyr
NM_001385197.1:c.2303C>A	NP_001372126.1:p.Ser768Tyr
NM_001385198.1:c.2303C>A	NP_001372127.1:p.Ser768Tyr
NM_001385199.1:c.2117C>A	NP_001372128.1:p.Ser706Tyr
NM_001385200.1:c.2303C>A	NP_001372129.1:p.Ser768Tyr
NM_001385201.1:c.2105C>A	NP_001372130.1:p.Ser702Tyr
NM_001385202.1:c.2219C>A	NP_001372131.1:p.Ser740Tyr
NM_001385203.1:c.2303C>A	NP_001372132.1:p.Ser768Tyr
NM_001385204.1:c.2303C>A	NP_001372133.1:p.Ser768Tyr
NM_001385205.1:c.2213C>A	NP_001372134.1:p.Ser738Tyr
NM_001385206.1:c.2177C>A	NP_001372135.1:p.Ser726Tyr
NM_001385207.1:c.2285C>A	NP_001372136.1:p.Ser762Tyr