Canonical Allele Identifier: CA2582371429
Gene: TYK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10353946_10353947del , CM000681.2:g.10353946_10353947del GRCh38
NC_000019.9:g.10464622_10464623del , CM000681.1:g.10464622_10464623del GRCh37
NC_000019.8:g.10325622_10325623del NCBI36
NG_007872.1:g.31629_31630del , LRG_121:g.31629_31630del

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1257+98_*1257+99del ENSP00000514307.1:n.*1257+98_*1257+99del
ENST00000525976.6:c.2908+98_2908+99del ENSP00000434831.2:n.2908+98_2908+99del
ENST00000527481.3:c.2908+98_2908+99del ENSP00000466340.2:n.2908+98_2908+99del
ENST00000529370.6:n.4284+98_4284+99del
ENST00000529739.2:n.3420_3421del
ENST00000530829.2:c.*2459+98_*2459+99del ENSP00000436826.2:n.*2459+98_*2459+99del
ENST00000531836.6:c.2908+98_2908+99del ENSP00000436175.2:n.2908+98_2908+99del
ENST00000533334.2:c.*950+98_*950+99del ENSP00000432320.2:n.*950+98_*950+99del
ENST00000534228.2:n.4465_4466del
ENST00000699354.1:n.1010+98_1010+99del
ENST00000699355.1:c.*2111_*2112del ENSP00000514328.1:n.*2111_*2112del
ENST00000699356.1:n.3420_3421del
ENST00000699357.1:n.4465_4466del
ENST00000699358.1:c.2908+98_2908+99del ENSP00000514329.1:n.2908+98_2908+99del
ENST00000699359.1:c.114+98_114+99del
ENST00000699360.1:c.2908+98_2908+99del ENSP00000514331.1:n.2908+98_2908+99del
ENST00000699368.1:c.113-15_113-14del ENSP00000514335.1:n.113-15_113-14del
ENST00000525621.6:c.2908+98_2908+99del MANE Select ENSP00000431885.1:n.2908+98_2908+99del
ENST00000264818.10:c.2908+98_2908+99del ENSP00000264818.6:n.2908+98_2908+99del
ENST00000524462.5:c.2353+98_2353+99del ENSP00000433203.1:n.2353+98_2353+99del
ENST00000525621.5:c.2908+98_2908+99del ENSP00000431885.1:n.2908+98_2908+99del
ENST00000527481.2:c.204+98_204+99del
ENST00000529412.1:n.678_679del
ENST00000529739.1:c.-321_-320del ENSP00000436155.1:n.-321_-320del
ENST00000530560.5:c.337+98_337+99del ENSP00000465291.1:n.337+98_337+99del
ENST00000592137.1:n.62+98_62+99del
NM_003331.4:c.2908+98_2908+99del , LRG_121t1:c.2908+98_2908+99del NP_003322.3:n.2908+98_2908+99del
XM_011528245.1:c.2908+98_2908+99del XP_011526547.1:n.2908+98_2908+99del
XM_011528246.1:c.2611+98_2611+99del XP_011526548.1:n.2611+98_2611+99del
XM_011528247.1:c.2611+98_2611+99del XP_011526549.1:n.2611+98_2611+99del
XM_011528248.1:c.2908+98_2908+99del XP_011526550.1:n.2908+98_2908+99del
XM_011528249.1:c.1582+98_1582+99del XP_011526551.1:n.1582+98_1582+99del
XM_011528251.1:c.1165+98_1165+99del XP_011526553.1:n.1165+98_1165+99del
XM_011528246.3:c.2611+98_2611+99del XP_011526548.1:n.2611+98_2611+99del
XM_011528249.2:c.1582+98_1582+99del XP_011526551.1:n.1582+98_1582+99del
XR_001753750.1:n.3065+98_3065+99del
XR_001753751.1:n.3163_3164del
XR_002958353.1:n.4089_4090del
NM_003331.5:c.2908+98_2908+99del MANE Select NP_003322.3:n.2908+98_2908+99del
NM_001385197.1:c.2908+98_2908+99del NP_001372126.1:n.2908+98_2908+99del
NM_001385198.1:c.2908+98_2908+99del NP_001372127.1:n.2908+98_2908+99del
NM_001385199.1:c.2722+98_2722+99del NP_001372128.1:n.2722+98_2722+99del
NM_001385200.1:c.2905+98_2905+99del NP_001372129.1:n.2905+98_2905+99del
NM_001385201.1:c.2710+98_2710+99del NP_001372130.1:n.2710+98_2710+99del
NM_001385202.1:c.2824+98_2824+99del NP_001372131.1:n.2824+98_2824+99del
NM_001385203.1:c.2989+98_2989+99del NP_001372132.1:n.2989+98_2989+99del
NM_001385204.1:c.3118+98_3118+99del NP_001372133.1:n.3118+98_3118+99del
NM_001385205.1:c.2818+98_2818+99del NP_001372134.1:n.2818+98_2818+99del
NM_001385206.1:c.2782+98_2782+99del NP_001372135.1:n.2782+98_2782+99del
NM_001385207.1:c.2890+98_2890+99del NP_001372136.1:n.2890+98_2890+99del