Canonical Allele Identifier: CA505373417

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464746G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354070G>A , CM000681.2:g.10354070G>A	GRCh38
NC_000019.9:g.10464746G>A , CM000681.1:g.10464746G>A	GRCh37
NC_000019.8:g.10325746G>A	NCBI36
NG_007872.1:g.31503C>T , LRG_121:g.31503C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1229C>T	ENSP00000514307.1:n.*1229C>T
ENST00000525976.6:c.2880C>T	ENSP00000434831.2:p.Ile960=
ENST00000527481.3:c.2880C>T	ENSP00000466340.2:p.Ile960=
ENST00000529370.6:n.4256C>T
ENST00000529739.2:n.3294C>T
ENST00000530829.2:c.*2431C>T	ENSP00000436826.2:n.*2431C>T
ENST00000531836.6:c.2880C>T	ENSP00000436175.2:p.Ile960=
ENST00000533334.2:c.*922C>T	ENSP00000432320.2:n.*922C>T
ENST00000534228.2:n.4339C>T
ENST00000699354.1:n.982C>T
ENST00000699355.1:c.*1985C>T	ENSP00000514328.1:n.*1985C>T
ENST00000699356.1:n.3294C>T
ENST00000699357.1:n.4339C>T
ENST00000699358.1:c.2880C>T	ENSP00000514329.1:p.Ile960=
ENST00000699359.1:c.86C>T
ENST00000699360.1:c.2880C>T	ENSP00000514331.1:p.Ile960=
ENST00000699368.1:c.84C>T	ENSP00000514335.1:p.Ile28=
ENST00000525621.6:c.2880C>T MANE Select	ENSP00000431885.1:p.Ile960=
ENST00000264818.10:c.2880C>T	ENSP00000264818.6:p.Ile960=
ENST00000524462.5:c.2325C>T	ENSP00000433203.1:p.Ile775=
ENST00000525621.5:c.2880C>T	ENSP00000431885.1:p.Ile960=
ENST00000527481.2:c.176C>T
ENST00000529412.1:n.552C>T
ENST00000529739.1:c.-447C>T	ENSP00000436155.1:n.-447C>T
ENST00000530560.5:c.309C>T	ENSP00000465291.1:p.Ile103=
ENST00000592137.1:n.34C>T
NM_003331.4:c.2880C>T , LRG_121t1:c.2880C>T	NP_003322.3:p.Ile960=
XM_011528245.1:c.2880C>T	XP_011526547.1:p.Ile960=
XM_011528246.1:c.2583C>T	XP_011526548.1:p.Ile861=
XM_011528247.1:c.2583C>T	XP_011526549.1:p.Ile861=
XM_011528248.1:c.2880C>T	XP_011526550.1:p.Ile960=
XM_011528249.1:c.1554C>T	XP_011526551.1:p.Ile518=
XM_011528251.1:c.1137C>T	XP_011526553.1:p.Ile379=
XM_011528246.3:c.2583C>T	XP_011526548.1:p.Ile861=
XM_011528249.2:c.1554C>T	XP_011526551.1:p.Ile518=
XR_001753750.1:n.3037C>T
XR_001753751.1:n.3037C>T
XR_002958353.1:n.3963C>T
NM_003331.5:c.2880C>T MANE Select	NP_003322.3:p.Ile960=
NM_001385197.1:c.2880C>T	NP_001372126.1:p.Ile960=
NM_001385198.1:c.2880C>T	NP_001372127.1:p.Ile960=
NM_001385199.1:c.2694C>T	NP_001372128.1:p.Ile898=
NM_001385200.1:c.2877C>T	NP_001372129.1:p.Ile959=
NM_001385201.1:c.2682C>T	NP_001372130.1:p.Ile894=
NM_001385202.1:c.2796C>T	NP_001372131.1:p.Ile932=
NM_001385203.1:c.2961C>T	NP_001372132.1:p.Ile987=
NM_001385204.1:c.3090C>T	NP_001372133.1:p.Ile1030=
NM_001385205.1:c.2790C>T	NP_001372134.1:p.Ile930=
NM_001385206.1:c.2754C>T	NP_001372135.1:p.Ile918=
NM_001385207.1:c.2862C>T	NP_001372136.1:p.Ile954=