Canonical Allele Identifier: CA993441138

Gene: TYK2

Linked Data

• dbSNP Id: rs2088359096
• gnomAD v3: 19-10352167-GT-G
• gnomAD v4: 19-10352167-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352169del , CM000681.2:g.10352169del	GRCh38
NC_000019.9:g.10462845del , CM000681.1:g.10462845del	GRCh37
NC_000019.8:g.10323845del	NCBI36
NG_007872.1:g.33405del , LRG_121:g.33405del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1667+266del	ENSP00000514307.1:n.*1667+266del
ENST00000525976.6:c.3318+266del	ENSP00000434831.2:n.3318+266del
ENST00000527481.3:c.*88+266del	ENSP00000466340.2:n.*88+266del
ENST00000529370.6:n.4694+266del
ENST00000529739.2:n.4127+266del
ENST00000530829.2:c.*2869+266del	ENSP00000436826.2:n.*2869+266del
ENST00000531836.6:c.3318+266del	ENSP00000436175.2:n.3318+266del
ENST00000533334.2:c.*1242+758del	ENSP00000432320.2:n.*1242+758del
ENST00000534228.2:n.5054+758del
ENST00000699354.1:n.1420+266del
ENST00000699355.1:c.*2818+266del	ENSP00000514328.1:n.*2818+266del
ENST00000699356.1:n.4127+266del
ENST00000699357.1:n.5172+266del
ENST00000699358.1:c.3200+758del	ENSP00000514329.1:n.3200+758del
ENST00000699359.1:c.492+266del
ENST00000699360.1:c.3276+266del	ENSP00000514331.1:n.3276+266del
ENST00000699361.1:n.352+266del
ENST00000699362.1:c.214+266del	ENSP00000514332.1:n.214+266del
ENST00000699363.1:c.214+266del	ENSP00000514333.1:n.214+266del
ENST00000699364.1:n.318+266del
ENST00000699365.1:c.387+266del	ENSP00000514334.1:n.387+266del
ENST00000699366.1:n.112-1200del
ENST00000699367.1:n.112-1006del
ENST00000699368.1:c.805+266del	ENSP00000514335.1:n.805+266del
ENST00000525621.6:c.3318+266del MANE Select	ENSP00000431885.1:n.3318+266del
ENST00000264818.10:c.3318+266del	ENSP00000264818.6:n.3318+266del
ENST00000524462.5:c.2763+266del	ENSP00000433203.1:n.2763+266del
ENST00000525621.5:c.3318+266del	ENSP00000431885.1:n.3318+266del
ENST00000525976.5:c.59+266del
ENST00000527481.2:c.495+266del
ENST00000529422.1:n.116+854del
ENST00000530220.1:n.331+758del
ENST00000530560.5:c.338-1200del	ENSP00000465291.1:n.338-1200del
ENST00000592137.1:n.472+266del
NM_003331.4:c.3318+266del , LRG_121t1:c.3318+266del	NP_003322.3:n.3318+266del
XM_011528245.1:c.3318+266del	XP_011526547.1:n.3318+266del
XM_011528246.1:c.3021+266del	XP_011526548.1:n.3021+266del
XM_011528247.1:c.3021+266del	XP_011526549.1:n.3021+266del
XM_011528248.1:c.3200+758del	XP_011526550.1:n.3200+758del
XM_011528249.1:c.1992+266del	XP_011526551.1:n.1992+266del
XM_011528251.1:c.1575+266del	XP_011526553.1:n.1575+266del
XM_011528246.3:c.3021+266del	XP_011526548.1:n.3021+266del
XM_011528249.2:c.1992+266del	XP_011526551.1:n.1992+266del
XR_001753750.1:n.3357+758del
XR_001753751.1:n.3870+266del
XR_002958353.1:n.4796+266del
NM_003331.5:c.3318+266del MANE Select	NP_003322.3:n.3318+266del
NM_001385197.1:c.3318+266del	NP_001372126.1:n.3318+266del
NM_001385198.1:c.3168+790del	NP_001372127.1:n.3168+790del
NM_001385199.1:c.3132+266del	NP_001372128.1:n.3132+266del
NM_001385200.1:c.3315+266del	NP_001372129.1:n.3315+266del
NM_001385201.1:c.3120+266del	NP_001372130.1:n.3120+266del
NM_001385202.1:c.3234+266del	NP_001372131.1:n.3234+266del
NM_001385203.1:c.3399+266del	NP_001372132.1:n.3399+266del
NM_001385204.1:c.3528+266del	NP_001372133.1:n.3528+266del
NM_001385205.1:c.3228+266del	NP_001372134.1:n.3228+266del
NM_001385206.1:c.3192+266del	NP_001372135.1:n.3192+266del
NM_001385207.1:c.3300+266del	NP_001372136.1:n.3300+266del