Canonical Allele Identifier: CA2322387825
Gene: TYK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10353844C= , CM000681.2:g.10353844C= GRCh38
NC_000019.9:g.10464520C= , CM000681.1:g.10464520C= GRCh37
NC_000019.8:g.10325520C= NCBI36
NG_007872.1:g.31729G= , LRG_121:g.31729G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1258-198G= ENSP00000514307.1:n.*1258-198G=
ENST00000525976.6:c.2909-198G= ENSP00000434831.2:n.2909-198G=
ENST00000527481.3:c.2908+198G= ENSP00000466340.2:n.2908+198G=
ENST00000529370.6:n.4285-198G=
ENST00000529739.2:n.3520G=
ENST00000530829.2:c.*2460-198G= ENSP00000436826.2:n.*2460-198G=
ENST00000531836.6:c.2909-198G= ENSP00000436175.2:n.2909-198G=
ENST00000533334.2:c.*951-198G= ENSP00000432320.2:n.*951-198G=
ENST00000534228.2:n.4565G=
ENST00000699354.1:n.1011-198G=
ENST00000699355.1:c.*2211G= ENSP00000514328.1:n.*2211G=
ENST00000699356.1:n.3520G=
ENST00000699357.1:n.4565G=
ENST00000699358.1:c.2909-198G= ENSP00000514329.1:n.2909-198G=
ENST00000699359.1:c.115-198G=
ENST00000699360.1:c.2909-198G= ENSP00000514331.1:n.2909-198G=
ENST00000699365.1:c.-54G= ENSP00000514334.1:n.-54G=
ENST00000699366.1:n.81G=
ENST00000699367.1:n.81G=
ENST00000699368.1:c.198G= ENSP00000514335.1:n.198G=
ENST00000525621.6:c.2909-198G= MANE Select ENSP00000431885.1:n.2909-198G=
ENST00000264818.10:c.2909-198G= ENSP00000264818.6:n.2909-198G=
ENST00000524462.5:c.2354-198G= ENSP00000433203.1:n.2354-198G=
ENST00000525621.5:c.2909-198G= ENSP00000431885.1:n.2909-198G=
ENST00000527481.2:c.204+198G=
ENST00000529739.1:c.-221G= ENSP00000436155.1:n.-221G=
ENST00000530560.5:c.337+198G= ENSP00000465291.1:n.337+198G=
ENST00000592137.1:n.63-198G=
NM_003331.4:c.2909-198G= , LRG_121t1:c.2909-198G= NP_003322.3:n.2909-198G=
XM_011528245.1:c.2909-198G= XP_011526547.1:n.2909-198G=
XM_011528246.1:c.2612-198G= XP_011526548.1:n.2612-198G=
XM_011528247.1:c.2612-198G= XP_011526549.1:n.2612-198G=
XM_011528248.1:c.2909-198G= XP_011526550.1:n.2909-198G=
XM_011528249.1:c.1583-198G= XP_011526551.1:n.1583-198G=
XM_011528251.1:c.1166-198G= XP_011526553.1:n.1166-198G=
XM_011528246.3:c.2612-198G= XP_011526548.1:n.2612-198G=
XM_011528249.2:c.1583-198G= XP_011526551.1:n.1583-198G=
XR_001753750.1:n.3066-198G=
XR_001753751.1:n.3263G=
XR_002958353.1:n.4189G=
NM_003331.5:c.2909-198G= MANE Select NP_003322.3:n.2909-198G=
NM_001385197.1:c.2909-198G= NP_001372126.1:n.2909-198G=
NM_001385198.1:c.2909-198G= NP_001372127.1:n.2909-198G=
NM_001385199.1:c.2723-198G= NP_001372128.1:n.2723-198G=
NM_001385200.1:c.2906-198G= NP_001372129.1:n.2906-198G=
NM_001385201.1:c.2711-198G= NP_001372130.1:n.2711-198G=
NM_001385202.1:c.2825-198G= NP_001372131.1:n.2825-198G=
NM_001385203.1:c.2990-198G= NP_001372132.1:n.2990-198G=
NM_001385204.1:c.3119-198G= NP_001372133.1:n.3119-198G=
NM_001385205.1:c.2819-198G= NP_001372134.1:n.2819-198G=
NM_001385206.1:c.2783-198G= NP_001372135.1:n.2783-198G=
NM_001385207.1:c.2891-198G= NP_001372136.1:n.2891-198G=