Canonical Allele Identifier: CA2322391692

Gene: TYK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10361760_10361761delinsGC , CM000681.2:g.10361760_10361761delinsGC	GRCh38
NC_000019.9:g.10472436_10472437delinsGC , CM000681.1:g.10472436_10472437delinsGC	GRCh37
NC_000019.8:g.10333436_10333437delinsGC	NCBI36
NG_007872.1:g.23812_23813delinsGC , LRG_121:g.23812_23813delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*308+9_*308+10delinsGC	ENSP00000514307.1:n.*308+9_*308+10delinsGC
ENST00000525976.6:c.1959+9_1959+10delinsGC	ENSP00000434831.2:n.1959+9_1959+10delinsGC
ENST00000527481.3:c.1959+9_1959+10delinsGC	ENSP00000466340.2:n.1959+9_1959+10delinsGC
ENST00000529370.6:n.2290+9_2290+10delinsGC
ENST00000529739.2:n.2373+9_2373+10delinsGC
ENST00000530829.2:c.*1510+9_*1510+10delinsGC	ENSP00000436826.2:n.*1510+9_*1510+10delinsGC
ENST00000531836.6:c.1959+9_1959+10delinsGC	ENSP00000436175.2:n.1959+9_1959+10delinsGC
ENST00000533334.2:c.1959+9_1959+10delinsGC	ENSP00000432320.2:n.1959+9_1959+10delinsGC
ENST00000534228.2:n.2373+9_2373+10delinsGC
ENST00000699355.1:c.*19+9_*19+10delinsGC	ENSP00000514328.1:n.*19+9_*19+10delinsGC
ENST00000699356.1:n.2373+9_2373+10delinsGC
ENST00000699357.1:n.2373+9_2373+10delinsGC
ENST00000699358.1:c.1959+9_1959+10delinsGC	ENSP00000514329.1:n.1959+9_1959+10delinsGC
ENST00000699360.1:c.1959+9_1959+10delinsGC	ENSP00000514331.1:n.1959+9_1959+10delinsGC
ENST00000525621.6:c.1959+9_1959+10delinsGC MANE Select	ENSP00000431885.1:n.1959+9_1959+10delinsGC
ENST00000264818.10:c.1959+9_1959+10delinsGC	ENSP00000264818.6:n.1959+9_1959+10delinsGC
ENST00000524462.5:c.1404+9_1404+10delinsGC	ENSP00000433203.1:n.1404+9_1404+10delinsGC
ENST00000525621.5:c.1959+9_1959+10delinsGC	ENSP00000431885.1:n.1959+9_1959+10delinsGC
ENST00000529370.5:c.1959+9_1959+10delinsGC	ENSP00000432728.1:n.1959+9_1959+10delinsGC
ENST00000531620.1:n.292+9_292+10delinsGC
ENST00000533334.1:c.136+9_136+10delinsGC
NM_003331.4:c.1959+9_1959+10delinsGC , LRG_121t1:c.1959+9_1959+10delinsGC	NP_003322.3:n.1959+9_1959+10delinsGC
XM_011528245.1:c.1959+9_1959+10delinsGC	XP_011526547.1:n.1959+9_1959+10delinsGC
XM_011528246.1:c.1662+9_1662+10delinsGC	XP_011526548.1:n.1662+9_1662+10delinsGC
XM_011528247.1:c.1662+9_1662+10delinsGC	XP_011526549.1:n.1662+9_1662+10delinsGC
XM_011528248.1:c.1959+9_1959+10delinsGC	XP_011526550.1:n.1959+9_1959+10delinsGC
XM_011528249.1:c.633+9_633+10delinsGC	XP_011526551.1:n.633+9_633+10delinsGC
XM_011528250.1:c.1959+9_1959+10delinsGC	XP_011526552.1:n.1959+9_1959+10delinsGC
XM_011528251.1:c.216+9_216+10delinsGC	XP_011526553.1:n.216+9_216+10delinsGC
XM_011528252.1:c.*19+9_*19+10delinsGC	XP_011526554.1:n.*19+9_*19+10delinsGC
XM_011528246.3:c.1662+9_1662+10delinsGC	XP_011526548.1:n.1662+9_1662+10delinsGC
XM_011528249.2:c.633+9_633+10delinsGC	XP_011526551.1:n.633+9_633+10delinsGC
XR_001753750.1:n.2116+9_2116+10delinsGC
XR_001753751.1:n.2116+9_2116+10delinsGC
XR_001753752.1:n.2116+9_2116+10delinsGC
XR_002958353.1:n.1997+9_1997+10delinsGC
NM_003331.5:c.1959+9_1959+10delinsGC MANE Select	NP_003322.3:n.1959+9_1959+10delinsGC
NM_001385197.1:c.1959+9_1959+10delinsGC	NP_001372126.1:n.1959+9_1959+10delinsGC
NM_001385198.1:c.1959+9_1959+10delinsGC	NP_001372127.1:n.1959+9_1959+10delinsGC
NM_001385199.1:c.1774-163_1774-162delinsGC	NP_001372128.1:n.1774-163_1774-162delinsGC
NM_001385200.1:c.1959+9_1959+10delinsGC	NP_001372129.1:n.1959+9_1959+10delinsGC
NM_001385201.1:c.1761+9_1761+10delinsGC	NP_001372130.1:n.1761+9_1761+10delinsGC
NM_001385202.1:c.1875+9_1875+10delinsGC	NP_001372131.1:n.1875+9_1875+10delinsGC
NM_001385203.1:c.1959+9_1959+10delinsGC	NP_001372132.1:n.1959+9_1959+10delinsGC
NM_001385204.1:c.1959+9_1959+10delinsGC	NP_001372133.1:n.1959+9_1959+10delinsGC
NM_001385205.1:c.1869+9_1869+10delinsGC	NP_001372134.1:n.1869+9_1869+10delinsGC
NM_001385206.1:c.1833+9_1833+10delinsGC	NP_001372135.1:n.1833+9_1833+10delinsGC
NM_001385207.1:c.1941+9_1941+10delinsGC	NP_001372136.1:n.1941+9_1941+10delinsGC