Canonical Allele Identifier: CA2322386909
Gene: TYK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10352123G= , CM000681.2:g.10352123G= GRCh38
NC_000019.9:g.10462799G= , CM000681.1:g.10462799G= GRCh37
NC_000019.8:g.10323799G= NCBI36
NG_007872.1:g.33450C= , LRG_121:g.33450C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1667+311C= ENSP00000514307.1:n.*1667+311C=
ENST00000525976.6:c.3318+311C= ENSP00000434831.2:n.3318+311C=
ENST00000527481.3:c.*88+311C= ENSP00000466340.2:n.*88+311C=
ENST00000529370.6:n.4694+311C=
ENST00000529739.2:n.4127+311C=
ENST00000530829.2:c.*2869+311C= ENSP00000436826.2:n.*2869+311C=
ENST00000531836.6:c.3318+311C= ENSP00000436175.2:n.3318+311C=
ENST00000533334.2:c.*1242+803C= ENSP00000432320.2:n.*1242+803C=
ENST00000534228.2:n.5054+803C=
ENST00000699354.1:n.1420+311C=
ENST00000699355.1:c.*2818+311C= ENSP00000514328.1:n.*2818+311C=
ENST00000699356.1:n.4127+311C=
ENST00000699357.1:n.5172+311C=
ENST00000699358.1:c.3200+803C= ENSP00000514329.1:n.3200+803C=
ENST00000699359.1:c.492+311C=
ENST00000699360.1:c.3276+311C= ENSP00000514331.1:n.3276+311C=
ENST00000699361.1:n.352+311C=
ENST00000699362.1:c.214+311C= ENSP00000514332.1:n.214+311C=
ENST00000699363.1:c.214+311C= ENSP00000514333.1:n.214+311C=
ENST00000699364.1:n.318+311C=
ENST00000699365.1:c.387+311C= ENSP00000514334.1:n.387+311C=
ENST00000699366.1:n.112-1155C=
ENST00000699367.1:n.112-961C=
ENST00000699368.1:c.805+311C= ENSP00000514335.1:n.805+311C=
ENST00000525621.6:c.3318+311C= MANE Select ENSP00000431885.1:n.3318+311C=
ENST00000264818.10:c.3318+311C= ENSP00000264818.6:n.3318+311C=
ENST00000524462.5:c.2763+311C= ENSP00000433203.1:n.2763+311C=
ENST00000525621.5:c.3318+311C= ENSP00000431885.1:n.3318+311C=
ENST00000525976.5:c.59+311C=
ENST00000527481.2:c.495+311C=
ENST00000529422.1:n.117-830C=
ENST00000530220.1:n.331+803C=
ENST00000530560.5:c.338-1155C= ENSP00000465291.1:n.338-1155C=
ENST00000592137.1:n.472+311C=
NM_003331.4:c.3318+311C= , LRG_121t1:c.3318+311C= NP_003322.3:n.3318+311C=
XM_011528245.1:c.3318+311C= XP_011526547.1:n.3318+311C=
XM_011528246.1:c.3021+311C= XP_011526548.1:n.3021+311C=
XM_011528247.1:c.3021+311C= XP_011526549.1:n.3021+311C=
XM_011528248.1:c.3200+803C= XP_011526550.1:n.3200+803C=
XM_011528249.1:c.1992+311C= XP_011526551.1:n.1992+311C=
XM_011528251.1:c.1575+311C= XP_011526553.1:n.1575+311C=
XM_011528246.3:c.3021+311C= XP_011526548.1:n.3021+311C=
XM_011528249.2:c.1992+311C= XP_011526551.1:n.1992+311C=
XR_001753750.1:n.3357+803C=
XR_001753751.1:n.3870+311C=
XR_002958353.1:n.4796+311C=
NM_003331.5:c.3318+311C= MANE Select NP_003322.3:n.3318+311C=
NM_001385197.1:c.3318+311C= NP_001372126.1:n.3318+311C=
NM_001385198.1:c.3168+835C= NP_001372127.1:n.3168+835C=
NM_001385199.1:c.3132+311C= NP_001372128.1:n.3132+311C=
NM_001385200.1:c.3315+311C= NP_001372129.1:n.3315+311C=
NM_001385201.1:c.3120+311C= NP_001372130.1:n.3120+311C=
NM_001385202.1:c.3234+311C= NP_001372131.1:n.3234+311C=
NM_001385203.1:c.3399+311C= NP_001372132.1:n.3399+311C=
NM_001385204.1:c.3528+311C= NP_001372133.1:n.3528+311C=
NM_001385205.1:c.3228+311C= NP_001372134.1:n.3228+311C=
NM_001385206.1:c.3192+311C= NP_001372135.1:n.3192+311C=
NM_001385207.1:c.3300+311C= NP_001372136.1:n.3300+311C=