Canonical Allele Identifier: CA2582372537

Gene: TYK2

Linked Data

• gnomAD v4: 19-10357886-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10357891del , CM000681.2:g.10357891del	GRCh38
NC_000019.9:g.10468567del , CM000681.1:g.10468567del	GRCh37
NC_000019.8:g.10329567del	NCBI36
NG_007872.1:g.27686del , LRG_121:g.27686del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*692del	ENSP00000514307.1:n.*692del
ENST00000525976.6:c.2343del	ENSP00000434831.2:p.Glu782AsnfsTer10
ENST00000527481.3:c.2343del	ENSP00000466340.2:p.Glu782AsnfsTer10
ENST00000529370.6:n.2674del
ENST00000529739.2:n.2757del
ENST00000530829.2:c.*1894del	ENSP00000436826.2:n.*1894del
ENST00000531836.6:c.2343del	ENSP00000436175.2:p.Glu782AsnfsTer10
ENST00000533334.2:c.*385del	ENSP00000432320.2:n.*385del
ENST00000534228.2:n.2757del
ENST00000699354.1:n.445del
ENST00000699355.1:c.*403del	ENSP00000514328.1:n.*403del
ENST00000699356.1:n.2757del
ENST00000699357.1:n.2757del
ENST00000699358.1:c.2343del	ENSP00000514329.1:p.Glu782AsnfsTer10
ENST00000699360.1:c.2343del	ENSP00000514331.1:p.Glu782AsnfsTer10
ENST00000525621.6:c.2343del MANE Select	ENSP00000431885.1:p.Glu782AsnfsTer10
ENST00000264818.10:c.2343del	ENSP00000264818.6:p.Glu782AsnfsTer10
ENST00000524462.5:c.1788del	ENSP00000433203.1:p.Glu597AsnfsTer10
ENST00000525621.5:c.2343del	ENSP00000431885.1:p.Glu782AsnfsTer10
ENST00000529370.5:c.2343del	ENSP00000432728.1:p.Glu782AsnfsTer10
ENST00000529412.1:n.15del
ENST00000533334.1:c.632del
NM_003331.4:c.2343del , LRG_121t1:c.2343del	NP_003322.3:p.Glu782AsnfsTer10
XM_011528245.1:c.2343del	XP_011526547.1:p.Glu782AsnfsTer10
XM_011528246.1:c.2046del	XP_011526548.1:p.Glu683AsnfsTer10
XM_011528247.1:c.2046del	XP_011526549.1:p.Glu683AsnfsTer10
XM_011528248.1:c.2343del	XP_011526550.1:p.Glu782AsnfsTer10
XM_011528249.1:c.1017del	XP_011526551.1:p.Glu340AsnfsTer10
XM_011528251.1:c.600del	XP_011526553.1:p.Glu201AsnfsTer10
XM_011528246.3:c.2046del	XP_011526548.1:p.Glu683AsnfsTer10
XM_011528249.2:c.1017del	XP_011526551.1:p.Glu340AsnfsTer10
XR_001753750.1:n.2500del
XR_001753751.1:n.2500del
XR_001753752.1:n.2612del
XR_002958353.1:n.2381del
NM_003331.5:c.2343del MANE Select	NP_003322.3:p.Glu782AsnfsTer10
NM_001385197.1:c.2343del	NP_001372126.1:p.Glu782AsnfsTer10
NM_001385198.1:c.2343del	NP_001372127.1:p.Glu782AsnfsTer10
NM_001385199.1:c.2157del	NP_001372128.1:p.Glu720AsnfsTer10
NM_001385200.1:c.2343del	NP_001372129.1:p.Glu782AsnfsTer10
NM_001385201.1:c.2145del	NP_001372130.1:p.Glu716AsnfsTer10
NM_001385202.1:c.2259del	NP_001372131.1:p.Glu754AsnfsTer10
NM_001385203.1:c.2343del	NP_001372132.1:p.Glu782AsnfsTer10
NM_001385204.1:c.2343del	NP_001372133.1:p.Glu782AsnfsTer10
NM_001385205.1:c.2253del	NP_001372134.1:p.Glu752AsnfsTer10
NM_001385206.1:c.2217del	NP_001372135.1:p.Glu740AsnfsTer10
NM_001385207.1:c.2325del	NP_001372136.1:p.Glu776AsnfsTer10