Canonical Allele Identifier: CA2582370045

Gene: TYK2

Linked Data

• gnomAD v4: 19-10352436-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352442_10352443del , CM000681.2:g.10352442_10352443del	GRCh38
NC_000019.9:g.10463118_10463119del , CM000681.1:g.10463118_10463119del	GRCh37
NC_000019.8:g.10324118_10324119del	NCBI36
NG_007872.1:g.33135_33136del , LRG_121:g.33135_33136del

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.*1663_*1664del	ENSP00000514307.1:n.*1663_*1664del
ENST00000525976.6:c.3314_3315del	ENSP00000434831.2:p.Pro1105HisfsTer?
ENST00000527481.3:c.*84_*85del	ENSP00000466340.2:n.*84_*85del
ENST00000529370.6:n.4690_4691del
ENST00000529739.2:n.4123_4124del
ENST00000530829.2:c.*2865_*2866del	ENSP00000436826.2:n.*2865_*2866del
ENST00000531836.6:c.3314_3315del	ENSP00000436175.2:p.Pro1105HisfsTer5
ENST00000533334.2:c.*1242+488_*1242+489del	ENSP00000432320.2:n.*1242+488_*1242+489de...
ENST00000534228.2:n.5054+488_5054+489del
ENST00000699354.1:n.1416_1417del
ENST00000699355.1:c.*2814_*2815del	ENSP00000514328.1:n.*2814_*2815del
ENST00000699356.1:n.4123_4124del
ENST00000699357.1:n.5168_5169del
ENST00000699358.1:c.3200+488_3200+489del	ENSP00000514329.1:n.3200+488_3200+489del
ENST00000699359.1:c.488_489del
ENST00000699360.1:c.3272_3273del	ENSP00000514331.1:p.Pro1091HisfsTer5
ENST00000699361.1:n.348_349del
ENST00000699362.1:c.210_211del	ENSP00000514332.1:n.210_211del
ENST00000699363.1:c.210_211del	ENSP00000514333.1:n.210_211del
ENST00000699364.1:n.314_315del
ENST00000699365.1:c.383_384del	ENSP00000514334.1:p.Pro128HisfsTer5
ENST00000699366.1:n.111+1376_111+1377del
ENST00000699367.1:n.112-1276_112-1275del
ENST00000699368.1:c.801_802del	ENSP00000514335.1:n.801_802del
ENST00000525621.6:c.3314_3315del MANE Select	ENSP00000431885.1:p.Pro1105HisfsTer5
ENST00000264818.10:c.3314_3315del	ENSP00000264818.6:p.Pro1105HisfsTer5
ENST00000524462.5:c.2759_2760del	ENSP00000433203.1:p.Pro920HisfsTer5
ENST00000525621.5:c.3314_3315del	ENSP00000431885.1:p.Pro1105HisfsTer5
ENST00000525976.5:c.55_56del
ENST00000527481.2:c.491_492del
ENST00000529422.1:n.116+584_116+585del
ENST00000529739.1:c.383_384del	ENSP00000436155.1:p.Pro128HisfsTer?
ENST00000530220.1:n.331+488_331+489del
ENST00000530560.5:c.338-1470_338-1469del	ENSP00000465291.1:n.338-1470_338-1469del
ENST00000592137.1:n.468_469del
NM_003331.4:c.3314_3315del , LRG_121t1:c.3314_3315del	NP_003322.3:p.Pro1105HisfsTer5
XM_011528245.1:c.3314_3315del	XP_011526547.1:p.Pro1105HisfsTer5
XM_011528246.1:c.3017_3018del	XP_011526548.1:p.Pro1006HisfsTer5
XM_011528247.1:c.3017_3018del	XP_011526549.1:p.Pro1006HisfsTer5
XM_011528248.1:c.3200+488_3200+489del	XP_011526550.1:n.3200+488_3200+489del
XM_011528249.1:c.1988_1989del	XP_011526551.1:p.Pro663HisfsTer5
XM_011528251.1:c.1571_1572del	XP_011526553.1:p.Pro524HisfsTer5
XM_011528246.3:c.3017_3018del	XP_011526548.1:p.Pro1006HisfsTer5
XM_011528249.2:c.1988_1989del	XP_011526551.1:p.Pro663HisfsTer5
XR_001753750.1:n.3357+488_3357+489del
XR_001753751.1:n.3866_3867del
XR_002958353.1:n.4792_4793del
NM_003331.5:c.3314_3315del MANE Select	NP_003322.3:p.Pro1105HisfsTer5
NM_001385197.1:c.3314_3315del	NP_001372126.1:p.Pro1105HisfsTer?
NM_001385198.1:c.3168+520_3168+521del	NP_001372127.1:n.3168+520_3168+521del
NM_001385199.1:c.3128_3129del	NP_001372128.1:p.Pro1043HisfsTer5
NM_001385200.1:c.3311_3312del	NP_001372129.1:p.Pro1104HisfsTer5
NM_001385201.1:c.3116_3117del	NP_001372130.1:p.Pro1039HisfsTer5
NM_001385202.1:c.3230_3231del	NP_001372131.1:p.Pro1077HisfsTer5
NM_001385203.1:c.3395_3396del	NP_001372132.1:p.Pro1132HisfsTer5
NM_001385204.1:c.3524_3525del	NP_001372133.1:p.Pro1175HisfsTer5
NM_001385205.1:c.3224_3225del	NP_001372134.1:p.Pro1075HisfsTer5
NM_001385206.1:c.3188_3189del	NP_001372135.1:p.Pro1063HisfsTer5
NM_001385207.1:c.3296_3297del	NP_001372136.1:p.Pro1099HisfsTer5