Canonical Allele Identifier: CA2322386899
Gene: TYK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10352104_10352106delinsGCT , CM000681.2:g.10352104_10352106delinsGCT GRCh38
NC_000019.9:g.10462780_10462782delinsGCT , CM000681.1:g.10462780_10462782delinsGCT GRCh37
NC_000019.8:g.10323780_10323782delinsGCT NCBI36
NG_007872.1:g.33467_33469delinsAGC , LRG_121:g.33467_33469delinsAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1667+328_*1667+330delinsAGC ENSP00000514307.1:n.*1667+328_*1667+330delinsAGC
ENST00000525976.6:c.3318+328_3318+330delinsAGC ENSP00000434831.2:n.3318+328_3318+330delinsAGC
ENST00000527481.3:c.*88+328_*88+330delinsAGC ENSP00000466340.2:n.*88+328_*88+330delinsAGC
ENST00000529370.6:n.4694+328_4694+330delinsAGC
ENST00000529739.2:n.4127+328_4127+330delinsAGC
ENST00000530829.2:c.*2869+328_*2869+330delinsAGC ENSP00000436826.2:n.*2869+328_*2869+330delinsAGC
ENST00000531836.6:c.3318+328_3318+330delinsAGC ENSP00000436175.2:n.3318+328_3318+330delinsAGC
ENST00000533334.2:c.*1242+820_*1242+822delinsAGC ENSP00000432320.2:n.*1242+820_*1242+822delinsAGC
ENST00000534228.2:n.5054+820_5054+822delinsAGC
ENST00000699354.1:n.1420+328_1420+330delinsAGC
ENST00000699355.1:c.*2818+328_*2818+330delinsAGC ENSP00000514328.1:n.*2818+328_*2818+330delinsAGC
ENST00000699356.1:n.4127+328_4127+330delinsAGC
ENST00000699357.1:n.5172+328_5172+330delinsAGC
ENST00000699358.1:c.3200+820_3200+822delinsAGC ENSP00000514329.1:n.3200+820_3200+822delinsAGC
ENST00000699359.1:c.492+328_492+330delinsAGC
ENST00000699360.1:c.3276+328_3276+330delinsAGC ENSP00000514331.1:n.3276+328_3276+330delinsAGC
ENST00000699361.1:n.352+328_352+330delinsAGC
ENST00000699362.1:c.214+328_214+330delinsAGC ENSP00000514332.1:n.214+328_214+330delinsAGC
ENST00000699363.1:c.214+328_214+330delinsAGC ENSP00000514333.1:n.214+328_214+330delinsAGC
ENST00000699364.1:n.318+328_318+330delinsAGC
ENST00000699365.1:c.387+328_387+330delinsAGC ENSP00000514334.1:n.387+328_387+330delinsAGC
ENST00000699366.1:n.112-1138_112-1136delinsAGC
ENST00000699367.1:n.112-944_112-942delinsAGC
ENST00000699368.1:c.805+328_805+330delinsAGC ENSP00000514335.1:n.805+328_805+330delinsAGC
ENST00000525621.6:c.3318+328_3318+330delinsAGC MANE Select ENSP00000431885.1:n.3318+328_3318+330delinsAGC
ENST00000264818.10:c.3318+328_3318+330delinsAGC ENSP00000264818.6:n.3318+328_3318+330delinsAGC
ENST00000524462.5:c.2763+328_2763+330delinsAGC ENSP00000433203.1:n.2763+328_2763+330delinsAGC
ENST00000525621.5:c.3318+328_3318+330delinsAGC ENSP00000431885.1:n.3318+328_3318+330delinsAGC
ENST00000525976.5:c.59+328_59+330delinsAGC
ENST00000527481.2:c.495+328_495+330delinsAGC
ENST00000529422.1:n.117-813_117-811delinsAGC
ENST00000530220.1:n.331+820_331+822delinsAGC
ENST00000530560.5:c.338-1138_338-1136delinsAGC ENSP00000465291.1:n.338-1138_338-1136delinsAGC
ENST00000592137.1:n.472+328_472+330delinsAGC
NM_003331.4:c.3318+328_3318+330delinsAGC , LRG_121t1:c.3318+328_3318+330delinsAGC NP_003322.3:n.3318+328_3318+330delinsAGC
XM_011528245.1:c.3318+328_3318+330delinsAGC XP_011526547.1:n.3318+328_3318+330delinsAGC
XM_011528246.1:c.3021+328_3021+330delinsAGC XP_011526548.1:n.3021+328_3021+330delinsAGC
XM_011528247.1:c.3021+328_3021+330delinsAGC XP_011526549.1:n.3021+328_3021+330delinsAGC
XM_011528248.1:c.3200+820_3200+822delinsAGC XP_011526550.1:n.3200+820_3200+822delinsAGC
XM_011528249.1:c.1992+328_1992+330delinsAGC XP_011526551.1:n.1992+328_1992+330delinsAGC
XM_011528251.1:c.1575+328_1575+330delinsAGC XP_011526553.1:n.1575+328_1575+330delinsAGC
XM_011528246.3:c.3021+328_3021+330delinsAGC XP_011526548.1:n.3021+328_3021+330delinsAGC
XM_011528249.2:c.1992+328_1992+330delinsAGC XP_011526551.1:n.1992+328_1992+330delinsAGC
XR_001753750.1:n.3357+820_3357+822delinsAGC
XR_001753751.1:n.3870+328_3870+330delinsAGC
XR_002958353.1:n.4796+328_4796+330delinsAGC
NM_003331.5:c.3318+328_3318+330delinsAGC MANE Select NP_003322.3:n.3318+328_3318+330delinsAGC
NM_001385197.1:c.3318+328_3318+330delinsAGC NP_001372126.1:n.3318+328_3318+330delinsAGC
NM_001385198.1:c.3168+852_3168+854delinsAGC NP_001372127.1:n.3168+852_3168+854delinsAGC
NM_001385199.1:c.3132+328_3132+330delinsAGC NP_001372128.1:n.3132+328_3132+330delinsAGC
NM_001385200.1:c.3315+328_3315+330delinsAGC NP_001372129.1:n.3315+328_3315+330delinsAGC
NM_001385201.1:c.3120+328_3120+330delinsAGC NP_001372130.1:n.3120+328_3120+330delinsAGC
NM_001385202.1:c.3234+328_3234+330delinsAGC NP_001372131.1:n.3234+328_3234+330delinsAGC
NM_001385203.1:c.3399+328_3399+330delinsAGC NP_001372132.1:n.3399+328_3399+330delinsAGC
NM_001385204.1:c.3528+328_3528+330delinsAGC NP_001372133.1:n.3528+328_3528+330delinsAGC
NM_001385205.1:c.3228+328_3228+330delinsAGC NP_001372134.1:n.3228+328_3228+330delinsAGC
NM_001385206.1:c.3192+328_3192+330delinsAGC NP_001372135.1:n.3192+328_3192+330delinsAGC
NM_001385207.1:c.3300+328_3300+330delinsAGC NP_001372136.1:n.3300+328_3300+330delinsAGC