Canonical Allele Identifier: CA403987887

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464762T>G (hg19) ; chr19:g.10354086T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354086T>G , CM000681.2:g.10354086T>G	GRCh38
NC_000019.9:g.10464762T>G , CM000681.1:g.10464762T>G	GRCh37
NC_000019.8:g.10325762T>G	NCBI36
NG_007872.1:g.31487A>C , LRG_121:g.31487A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1213A>C	ENSP00000514307.1:n.*1213A>C
ENST00000525976.6:c.2864A>C	ENSP00000434831.2:p.Tyr955Ser
ENST00000527481.3:c.2864A>C	ENSP00000466340.2:p.Tyr955Ser
ENST00000529370.6:n.4240A>C
ENST00000529739.2:n.3278A>C
ENST00000530829.2:c.*2415A>C	ENSP00000436826.2:n.*2415A>C
ENST00000531836.6:c.2864A>C	ENSP00000436175.2:p.Tyr955Ser
ENST00000533334.2:c.*906A>C	ENSP00000432320.2:n.*906A>C
ENST00000534228.2:n.4323A>C
ENST00000699354.1:n.966A>C
ENST00000699355.1:c.*1969A>C	ENSP00000514328.1:n.*1969A>C
ENST00000699356.1:n.3278A>C
ENST00000699357.1:n.4323A>C
ENST00000699358.1:c.2864A>C	ENSP00000514329.1:p.Tyr955Ser
ENST00000699359.1:c.70A>C
ENST00000699360.1:c.2864A>C	ENSP00000514331.1:p.Tyr955Ser
ENST00000699368.1:c.68A>C	ENSP00000514335.1:p.Tyr23Ser
ENST00000525621.6:c.2864A>C MANE Select	ENSP00000431885.1:p.Tyr955Ser
ENST00000264818.10:c.2864A>C	ENSP00000264818.6:p.Tyr955Ser
ENST00000524462.5:c.2309A>C	ENSP00000433203.1:p.Tyr770Ser
ENST00000525621.5:c.2864A>C	ENSP00000431885.1:p.Tyr955Ser
ENST00000527481.2:c.160A>C
ENST00000529412.1:n.536A>C
ENST00000530560.5:c.293A>C	ENSP00000465291.1:p.Tyr98Ser
ENST00000592137.1:n.18A>C
NM_003331.4:c.2864A>C , LRG_121t1:c.2864A>C	NP_003322.3:p.Tyr955Ser
XM_011528245.1:c.2864A>C	XP_011526547.1:p.Tyr955Ser
XM_011528246.1:c.2567A>C	XP_011526548.1:p.Tyr856Ser
XM_011528247.1:c.2567A>C	XP_011526549.1:p.Tyr856Ser
XM_011528248.1:c.2864A>C	XP_011526550.1:p.Tyr955Ser
XM_011528249.1:c.1538A>C	XP_011526551.1:p.Tyr513Ser
XM_011528251.1:c.1121A>C	XP_011526553.1:p.Tyr374Ser
XM_011528246.3:c.2567A>C	XP_011526548.1:p.Tyr856Ser
XM_011528249.2:c.1538A>C	XP_011526551.1:p.Tyr513Ser
XR_001753750.1:n.3021A>C
XR_001753751.1:n.3021A>C
XR_002958353.1:n.3947A>C
NM_003331.5:c.2864A>C MANE Select	NP_003322.3:p.Tyr955Ser
NM_001385197.1:c.2864A>C	NP_001372126.1:p.Tyr955Ser
NM_001385198.1:c.2864A>C	NP_001372127.1:p.Tyr955Ser
NM_001385199.1:c.2678A>C	NP_001372128.1:p.Tyr893Ser
NM_001385200.1:c.2861A>C	NP_001372129.1:p.Tyr954Ser
NM_001385201.1:c.2666A>C	NP_001372130.1:p.Tyr889Ser
NM_001385202.1:c.2780A>C	NP_001372131.1:p.Tyr927Ser
NM_001385203.1:c.2945A>C	NP_001372132.1:p.Tyr982Ser
NM_001385204.1:c.3074A>C	NP_001372133.1:p.Tyr1025Ser
NM_001385205.1:c.2774A>C	NP_001372134.1:p.Tyr925Ser
NM_001385206.1:c.2738A>C	NP_001372135.1:p.Tyr913Ser
NM_001385207.1:c.2846A>C	NP_001372136.1:p.Tyr949Ser