Canonical Allele Identifier: CA2582371267
Gene: TYK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10353827_10353830del , CM000681.2:g.10353827_10353830del GRCh38
NC_000019.9:g.10464503_10464506del , CM000681.1:g.10464503_10464506del GRCh37
NC_000019.8:g.10325503_10325506del NCBI36
NG_007872.1:g.31743_31746del , LRG_121:g.31743_31746del

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1258-184_*1258-181del ENSP00000514307.1:n.*1258-184_*1258-181del
ENST00000525976.6:c.2909-184_2909-181del ENSP00000434831.2:n.2909-184_2909-181del
ENST00000527481.3:c.2908+212_2908+215del ENSP00000466340.2:n.2908+212_2908+215del
ENST00000529370.6:n.4285-184_4285-181del
ENST00000529739.2:n.3534_3537del
ENST00000530829.2:c.*2460-184_*2460-181del ENSP00000436826.2:n.*2460-184_*2460-181del
ENST00000531836.6:c.2909-184_2909-181del ENSP00000436175.2:n.2909-184_2909-181del
ENST00000533334.2:c.*951-184_*951-181del ENSP00000432320.2:n.*951-184_*951-181del
ENST00000534228.2:n.4579_4582del
ENST00000699354.1:n.1011-184_1011-181del
ENST00000699355.1:c.*2225_*2228del ENSP00000514328.1:n.*2225_*2228del
ENST00000699356.1:n.3534_3537del
ENST00000699357.1:n.4579_4582del
ENST00000699358.1:c.2909-184_2909-181del ENSP00000514329.1:n.2909-184_2909-181del
ENST00000699359.1:c.115-184_115-181del
ENST00000699360.1:c.2909-184_2909-181del ENSP00000514331.1:n.2909-184_2909-181del
ENST00000699364.1:n.11_14del
ENST00000699365.1:c.-40_-37del ENSP00000514334.1:n.-40_-37del
ENST00000699366.1:n.95_98del
ENST00000699367.1:n.95_98del
ENST00000699368.1:c.212_215del ENSP00000514335.1:n.212_215del
ENST00000525621.6:c.2909-184_2909-181del MANE Select ENSP00000431885.1:n.2909-184_2909-181del
ENST00000264818.10:c.2909-184_2909-181del ENSP00000264818.6:n.2909-184_2909-181del
ENST00000524462.5:c.2354-184_2354-181del ENSP00000433203.1:n.2354-184_2354-181del
ENST00000525621.5:c.2909-184_2909-181del ENSP00000431885.1:n.2909-184_2909-181del
ENST00000527481.2:c.204+212_204+215del
ENST00000529739.1:c.-207_-204del ENSP00000436155.1:n.-207_-204del
ENST00000530560.5:c.337+212_337+215del ENSP00000465291.1:n.337+212_337+215del
ENST00000592137.1:n.63-184_63-181del
NM_003331.4:c.2909-184_2909-181del , LRG_121t1:c.2909-184_2909-181del NP_003322.3:n.2909-184_2909-181del
XM_011528245.1:c.2909-184_2909-181del XP_011526547.1:n.2909-184_2909-181del
XM_011528246.1:c.2612-184_2612-181del XP_011526548.1:n.2612-184_2612-181del
XM_011528247.1:c.2612-184_2612-181del XP_011526549.1:n.2612-184_2612-181del
XM_011528248.1:c.2909-184_2909-181del XP_011526550.1:n.2909-184_2909-181del
XM_011528249.1:c.1583-184_1583-181del XP_011526551.1:n.1583-184_1583-181del
XM_011528251.1:c.1166-184_1166-181del XP_011526553.1:n.1166-184_1166-181del
XM_011528246.3:c.2612-184_2612-181del XP_011526548.1:n.2612-184_2612-181del
XM_011528249.2:c.1583-184_1583-181del XP_011526551.1:n.1583-184_1583-181del
XR_001753750.1:n.3066-184_3066-181del
XR_001753751.1:n.3277_3280del
XR_002958353.1:n.4203_4206del
NM_003331.5:c.2909-184_2909-181del MANE Select NP_003322.3:n.2909-184_2909-181del
NM_001385197.1:c.2909-184_2909-181del NP_001372126.1:n.2909-184_2909-181del
NM_001385198.1:c.2909-184_2909-181del NP_001372127.1:n.2909-184_2909-181del
NM_001385199.1:c.2723-184_2723-181del NP_001372128.1:n.2723-184_2723-181del
NM_001385200.1:c.2906-184_2906-181del NP_001372129.1:n.2906-184_2906-181del
NM_001385201.1:c.2711-184_2711-181del NP_001372130.1:n.2711-184_2711-181del
NM_001385202.1:c.2825-184_2825-181del NP_001372131.1:n.2825-184_2825-181del
NM_001385203.1:c.2990-184_2990-181del NP_001372132.1:n.2990-184_2990-181del
NM_001385204.1:c.3119-184_3119-181del NP_001372133.1:n.3119-184_3119-181del
NM_001385205.1:c.2819-184_2819-181del NP_001372134.1:n.2819-184_2819-181del
NM_001385206.1:c.2783-184_2783-181del NP_001372135.1:n.2783-184_2783-181del
NM_001385207.1:c.2891-184_2891-181del NP_001372136.1:n.2891-184_2891-181del