Canonical Allele Identifier: CA505373741

Gene: TYK2

Linked Data

• gnomAD v4: 19-10354127-G-T
• MyVariant Identifiers: chr19:g.10464803G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354127G>T , CM000681.2:g.10354127G>T	GRCh38
NC_000019.9:g.10464803G>T , CM000681.1:g.10464803G>T	GRCh37
NC_000019.8:g.10325803G>T	NCBI36
NG_007872.1:g.31446C>A , LRG_121:g.31446C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1172C>A	ENSP00000514307.1:n.*1172C>A
ENST00000525976.6:c.2823C>A	ENSP00000434831.2:p.Arg941=
ENST00000527481.3:c.2823C>A	ENSP00000466340.2:p.Arg941=
ENST00000529370.6:n.4199C>A
ENST00000529739.2:n.3237C>A
ENST00000530829.2:c.*2374C>A	ENSP00000436826.2:n.*2374C>A
ENST00000531836.6:c.2823C>A	ENSP00000436175.2:p.Arg941=
ENST00000533334.2:c.*865C>A	ENSP00000432320.2:n.*865C>A
ENST00000534228.2:n.4282C>A
ENST00000699354.1:n.925C>A
ENST00000699355.1:c.*1928C>A	ENSP00000514328.1:n.*1928C>A
ENST00000699356.1:n.3237C>A
ENST00000699357.1:n.4282C>A
ENST00000699358.1:c.2823C>A	ENSP00000514329.1:p.Arg941=
ENST00000699359.1:c.29C>A
ENST00000699360.1:c.2823C>A	ENSP00000514331.1:p.Arg941=
ENST00000699368.1:c.27C>A	ENSP00000514335.1:p.Arg9=
ENST00000525621.6:c.2823C>A MANE Select	ENSP00000431885.1:p.Arg941=
ENST00000264818.10:c.2823C>A	ENSP00000264818.6:p.Arg941=
ENST00000524462.5:c.2268C>A	ENSP00000433203.1:p.Arg756=
ENST00000525621.5:c.2823C>A	ENSP00000431885.1:p.Arg941=
ENST00000527481.2:c.119C>A
ENST00000529412.1:n.495C>A
ENST00000530560.5:c.252C>A	ENSP00000465291.1:p.Arg84=
NM_003331.4:c.2823C>A , LRG_121t1:c.2823C>A	NP_003322.3:p.Arg941=
XM_011528245.1:c.2823C>A	XP_011526547.1:p.Arg941=
XM_011528246.1:c.2526C>A	XP_011526548.1:p.Arg842=
XM_011528247.1:c.2526C>A	XP_011526549.1:p.Arg842=
XM_011528248.1:c.2823C>A	XP_011526550.1:p.Arg941=
XM_011528249.1:c.1497C>A	XP_011526551.1:p.Arg499=
XM_011528251.1:c.1080C>A	XP_011526553.1:p.Arg360=
XM_011528246.3:c.2526C>A	XP_011526548.1:p.Arg842=
XM_011528249.2:c.1497C>A	XP_011526551.1:p.Arg499=
XR_001753750.1:n.2980C>A
XR_001753751.1:n.2980C>A
XR_002958353.1:n.3906C>A
NM_003331.5:c.2823C>A MANE Select	NP_003322.3:p.Arg941=
NM_001385197.1:c.2823C>A	NP_001372126.1:p.Arg941=
NM_001385198.1:c.2823C>A	NP_001372127.1:p.Arg941=
NM_001385199.1:c.2637C>A	NP_001372128.1:p.Arg879=
NM_001385200.1:c.2820C>A	NP_001372129.1:p.Arg940=
NM_001385201.1:c.2625C>A	NP_001372130.1:p.Arg875=
NM_001385202.1:c.2739C>A	NP_001372131.1:p.Arg913=
NM_001385203.1:c.2904C>A	NP_001372132.1:p.Arg968=
NM_001385204.1:c.3033C>A	NP_001372133.1:p.Arg1011=
NM_001385205.1:c.2733C>A	NP_001372134.1:p.Arg911=
NM_001385206.1:c.2697C>A	NP_001372135.1:p.Arg899=
NM_001385207.1:c.2805C>A	NP_001372136.1:p.Arg935=