Canonical Allele Identifier: CA505476465
Gene: TYK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10472545C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10361869C>T , CM000681.2:g.10361869C>T GRCh38
NC_000019.9:g.10472545C>T , CM000681.1:g.10472545C>T GRCh37
NC_000019.8:g.10333545C>T NCBI36
NG_007872.1:g.23704G>A , LRG_121:g.23704G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*209G>A ENSP00000514307.1:n.*209G>A
ENST00000525976.6:c.1860G>A ENSP00000434831.2:p.Lys620=
ENST00000527481.3:c.1860G>A ENSP00000466340.2:p.Lys620=
ENST00000529370.6:n.2191G>A
ENST00000529739.2:n.2274G>A
ENST00000530829.2:c.*1411G>A ENSP00000436826.2:n.*1411G>A
ENST00000531836.6:c.1860G>A ENSP00000436175.2:p.Lys620=
ENST00000533334.2:c.1860G>A ENSP00000432320.2:p.Lys620=
ENST00000534228.2:n.2274G>A
ENST00000699355.1:c.1774-33G>A ENSP00000514328.1:n.1774-33G>A
ENST00000699356.1:n.2274G>A
ENST00000699357.1:n.2274G>A
ENST00000699358.1:c.1860G>A ENSP00000514329.1:p.Lys620=
ENST00000699360.1:c.1860G>A ENSP00000514331.1:p.Lys620=
ENST00000525621.6:c.1860G>A MANE Select ENSP00000431885.1:p.Lys620=
ENST00000264818.10:c.1860G>A ENSP00000264818.6:p.Lys620=
ENST00000524462.5:c.1305G>A ENSP00000433203.1:p.Lys435=
ENST00000525621.5:c.1860G>A ENSP00000431885.1:p.Lys620=
ENST00000529370.5:c.1860G>A ENSP00000432728.1:p.Lys620=
ENST00000531620.1:n.193G>A
ENST00000533334.1:c.37G>A
NM_003331.4:c.1860G>A , LRG_121t1:c.1860G>A NP_003322.3:p.Lys620=
XM_011528245.1:c.1860G>A XP_011526547.1:p.Lys620=
XM_011528246.1:c.1563G>A XP_011526548.1:p.Lys521=
XM_011528247.1:c.1563G>A XP_011526549.1:p.Lys521=
XM_011528248.1:c.1860G>A XP_011526550.1:p.Lys620=
XM_011528249.1:c.534G>A XP_011526551.1:p.Lys178=
XM_011528250.1:c.1860G>A XP_011526552.1:p.Lys620=
XM_011528251.1:c.150-33G>A XP_011526553.1:n.150-33G>A
XM_011528252.1:c.1774-33G>A XP_011526554.1:n.1774-33G>A
XM_011528246.3:c.1563G>A XP_011526548.1:p.Lys521=
XM_011528249.2:c.534G>A XP_011526551.1:p.Lys178=
XR_001753750.1:n.2017G>A
XR_001753751.1:n.2017G>A
XR_001753752.1:n.2017G>A
XR_002958353.1:n.1931-33G>A
NM_003331.5:c.1860G>A MANE Select NP_003322.3:p.Lys620=
NM_001385197.1:c.1860G>A NP_001372126.1:p.Lys620=
NM_001385198.1:c.1860G>A NP_001372127.1:p.Lys620=
NM_001385199.1:c.1773+209G>A NP_001372128.1:n.1773+209G>A
NM_001385200.1:c.1860G>A NP_001372129.1:p.Lys620=
NM_001385201.1:c.1662G>A NP_001372130.1:p.Lys554=
NM_001385202.1:c.1809-33G>A NP_001372131.1:n.1809-33G>A
NM_001385203.1:c.1860G>A NP_001372132.1:p.Lys620=
NM_001385204.1:c.1860G>A NP_001372133.1:p.Lys620=
NM_001385205.1:c.1770G>A NP_001372134.1:p.Lys590=
NM_001385206.1:c.1734G>A NP_001372135.1:p.Lys578=
NM_001385207.1:c.1842G>A NP_001372136.1:p.Lys614=