Canonical Allele Identifier: CA403987680

Gene: TYK2

Linked Data

• dbSNP Id: rs1400138297
• gnomAD v2: 19-10464738-T-A
• gnomAD v4: 19-10354062-T-A
• MyVariant Identifiers: chr19:g.10464738T>A (hg19) ; chr19:g.10354062T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354062T>A , CM000681.2:g.10354062T>A	GRCh38
NC_000019.9:g.10464738T>A , CM000681.1:g.10464738T>A	GRCh37
NC_000019.8:g.10325738T>A	NCBI36
NG_007872.1:g.31511A>T , LRG_121:g.31511A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1237A>T	ENSP00000514307.1:n.*1237A>T
ENST00000525976.6:c.2888A>T	ENSP00000434831.2:p.Lys963Met
ENST00000527481.3:c.2888A>T	ENSP00000466340.2:p.Lys963Met
ENST00000529370.6:n.4264A>T
ENST00000529739.2:n.3302A>T
ENST00000530829.2:c.*2439A>T	ENSP00000436826.2:n.*2439A>T
ENST00000531836.6:c.2888A>T	ENSP00000436175.2:p.Lys963Met
ENST00000533334.2:c.*930A>T	ENSP00000432320.2:n.*930A>T
ENST00000534228.2:n.4347A>T
ENST00000699354.1:n.990A>T
ENST00000699355.1:c.*1993A>T	ENSP00000514328.1:n.*1993A>T
ENST00000699356.1:n.3302A>T
ENST00000699357.1:n.4347A>T
ENST00000699358.1:c.2888A>T	ENSP00000514329.1:p.Lys963Met
ENST00000699359.1:c.94A>T
ENST00000699360.1:c.2888A>T	ENSP00000514331.1:p.Lys963Met
ENST00000699368.1:c.92A>T	ENSP00000514335.1:p.Lys31Met
ENST00000525621.6:c.2888A>T MANE Select	ENSP00000431885.1:p.Lys963Met
ENST00000264818.10:c.2888A>T	ENSP00000264818.6:p.Lys963Met
ENST00000524462.5:c.2333A>T	ENSP00000433203.1:p.Lys778Met
ENST00000525621.5:c.2888A>T	ENSP00000431885.1:p.Lys963Met
ENST00000527481.2:c.184A>T
ENST00000529412.1:n.560A>T
ENST00000529739.1:c.-439A>T	ENSP00000436155.1:n.-439A>T
ENST00000530560.5:c.317A>T	ENSP00000465291.1:p.Lys106Met
ENST00000592137.1:n.42A>T
NM_003331.4:c.2888A>T , LRG_121t1:c.2888A>T	NP_003322.3:p.Lys963Met
XM_011528245.1:c.2888A>T	XP_011526547.1:p.Lys963Met
XM_011528246.1:c.2591A>T	XP_011526548.1:p.Lys864Met
XM_011528247.1:c.2591A>T	XP_011526549.1:p.Lys864Met
XM_011528248.1:c.2888A>T	XP_011526550.1:p.Lys963Met
XM_011528249.1:c.1562A>T	XP_011526551.1:p.Lys521Met
XM_011528251.1:c.1145A>T	XP_011526553.1:p.Lys382Met
XM_011528246.3:c.2591A>T	XP_011526548.1:p.Lys864Met
XM_011528249.2:c.1562A>T	XP_011526551.1:p.Lys521Met
XR_001753750.1:n.3045A>T
XR_001753751.1:n.3045A>T
XR_002958353.1:n.3971A>T
NM_003331.5:c.2888A>T MANE Select	NP_003322.3:p.Lys963Met
NM_001385197.1:c.2888A>T	NP_001372126.1:p.Lys963Met
NM_001385198.1:c.2888A>T	NP_001372127.1:p.Lys963Met
NM_001385199.1:c.2702A>T	NP_001372128.1:p.Lys901Met
NM_001385200.1:c.2885A>T	NP_001372129.1:p.Lys962Met
NM_001385201.1:c.2690A>T	NP_001372130.1:p.Lys897Met
NM_001385202.1:c.2804A>T	NP_001372131.1:p.Lys935Met
NM_001385203.1:c.2969A>T	NP_001372132.1:p.Lys990Met
NM_001385204.1:c.3098A>T	NP_001372133.1:p.Lys1033Met
NM_001385205.1:c.2798A>T	NP_001372134.1:p.Lys933Met
NM_001385206.1:c.2762A>T	NP_001372135.1:p.Lys921Met
NM_001385207.1:c.2870A>T	NP_001372136.1:p.Lys957Met