Canonical Allele Identifier: CA783141667
Gene: TYK2 HGNC NCBI

Linked Data

dbSNP Id: rs1286649978

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10352292_10352293insA , CM000681.2:g.10352292_10352293insA GRCh38
NC_000019.9:g.10462968_10462969insA , CM000681.1:g.10462968_10462969insA GRCh37
NC_000019.8:g.10323968_10323969insA NCBI36
NG_007872.1:g.33280_33281insT , LRG_121:g.33280_33281insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1667+141_*1667+142insT ENSP00000514307.1:n.*1667+141_*1667+142insT
ENST00000525976.6:c.3318+141_3318+142insT ENSP00000434831.2:n.3318+141_3318+142insT
ENST00000527481.3:c.*88+141_*88+142insT ENSP00000466340.2:n.*88+141_*88+142insT
ENST00000529370.6:n.4694+141_4694+142insT
ENST00000529739.2:n.4127+141_4127+142insT
ENST00000530829.2:c.*2869+141_*2869+142insT ENSP00000436826.2:n.*2869+141_*2869+142insT
ENST00000531836.6:c.3318+141_3318+142insT ENSP00000436175.2:n.3318+141_3318+142insT
ENST00000533334.2:c.*1242+633_*1242+634insT ENSP00000432320.2:n.*1242+633_*1242+634insT
ENST00000534228.2:n.5054+633_5054+634insT
ENST00000699354.1:n.1420+141_1420+142insT
ENST00000699355.1:c.*2818+141_*2818+142insT ENSP00000514328.1:n.*2818+141_*2818+142insT
ENST00000699356.1:n.4127+141_4127+142insT
ENST00000699357.1:n.5172+141_5172+142insT
ENST00000699358.1:c.3200+633_3200+634insT ENSP00000514329.1:n.3200+633_3200+634insT
ENST00000699359.1:c.492+141_492+142insT
ENST00000699360.1:c.3276+141_3276+142insT ENSP00000514331.1:n.3276+141_3276+142insT
ENST00000699361.1:n.352+141_352+142insT
ENST00000699362.1:c.214+141_214+142insT ENSP00000514332.1:n.214+141_214+142insT
ENST00000699363.1:c.214+141_214+142insT ENSP00000514333.1:n.214+141_214+142insT
ENST00000699364.1:n.318+141_318+142insT
ENST00000699365.1:c.387+141_387+142insT ENSP00000514334.1:n.387+141_387+142insT
ENST00000699366.1:n.112-1325_112-1324insT
ENST00000699367.1:n.112-1131_112-1130insT
ENST00000699368.1:c.805+141_805+142insT ENSP00000514335.1:n.805+141_805+142insT
ENST00000525621.6:c.3318+141_3318+142insT MANE Select ENSP00000431885.1:n.3318+141_3318+142insT
ENST00000264818.10:c.3318+141_3318+142insT ENSP00000264818.6:n.3318+141_3318+142insT
ENST00000524462.5:c.2763+141_2763+142insT ENSP00000433203.1:n.2763+141_2763+142insT
ENST00000525621.5:c.3318+141_3318+142insT ENSP00000431885.1:n.3318+141_3318+142insT
ENST00000525976.5:c.59+141_59+142insT
ENST00000527481.2:c.495+141_495+142insT
ENST00000529422.1:n.116+729_116+730insT
ENST00000530220.1:n.331+633_331+634insT
ENST00000530560.5:c.338-1325_338-1324insT ENSP00000465291.1:n.338-1325_338-1324insT
ENST00000592137.1:n.472+141_472+142insT
NM_003331.4:c.3318+141_3318+142insT , LRG_121t1:c.3318+141_3318+142insT NP_003322.3:n.3318+141_3318+142insT
XM_011528245.1:c.3318+141_3318+142insT XP_011526547.1:n.3318+141_3318+142insT
XM_011528246.1:c.3021+141_3021+142insT XP_011526548.1:n.3021+141_3021+142insT
XM_011528247.1:c.3021+141_3021+142insT XP_011526549.1:n.3021+141_3021+142insT
XM_011528248.1:c.3200+633_3200+634insT XP_011526550.1:n.3200+633_3200+634insT
XM_011528249.1:c.1992+141_1992+142insT XP_011526551.1:n.1992+141_1992+142insT
XM_011528251.1:c.1575+141_1575+142insT XP_011526553.1:n.1575+141_1575+142insT
XM_011528246.3:c.3021+141_3021+142insT XP_011526548.1:n.3021+141_3021+142insT
XM_011528249.2:c.1992+141_1992+142insT XP_011526551.1:n.1992+141_1992+142insT
XR_001753750.1:n.3357+633_3357+634insT
XR_001753751.1:n.3870+141_3870+142insT
XR_002958353.1:n.4796+141_4796+142insT
NM_003331.5:c.3318+141_3318+142insT MANE Select NP_003322.3:n.3318+141_3318+142insT
NM_001385197.1:c.3318+141_3318+142insT NP_001372126.1:n.3318+141_3318+142insT
NM_001385198.1:c.3168+665_3168+666insT NP_001372127.1:n.3168+665_3168+666insT
NM_001385199.1:c.3132+141_3132+142insT NP_001372128.1:n.3132+141_3132+142insT
NM_001385200.1:c.3315+141_3315+142insT NP_001372129.1:n.3315+141_3315+142insT
NM_001385201.1:c.3120+141_3120+142insT NP_001372130.1:n.3120+141_3120+142insT
NM_001385202.1:c.3234+141_3234+142insT NP_001372131.1:n.3234+141_3234+142insT
NM_001385203.1:c.3399+141_3399+142insT NP_001372132.1:n.3399+141_3399+142insT
NM_001385204.1:c.3528+141_3528+142insT NP_001372133.1:n.3528+141_3528+142insT
NM_001385205.1:c.3228+141_3228+142insT NP_001372134.1:n.3228+141_3228+142insT
NM_001385206.1:c.3192+141_3192+142insT NP_001372135.1:n.3192+141_3192+142insT
NM_001385207.1:c.3300+141_3300+142insT NP_001372136.1:n.3300+141_3300+142insT