Canonical Allele Identifier: CA9193083

Gene: TYK2

Linked Data

• dbSNP Id: rs546402387
• ExAC: 19:10468485 G / T
• gnomAD v2: 19-10468485-G-T
• gnomAD v3: 19-10357809-G-T
• gnomAD v4: 19-10357809-G-T
• MyVariant Identifiers: chr19:g.10468485G>T (hg19) ; chr19:g.10357809G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10357809G>T , CM000681.2:g.10357809G>T	GRCh38
NC_000019.9:g.10468485G>T , CM000681.1:g.10468485G>T	GRCh37
NC_000019.8:g.10329485G>T	NCBI36
NG_007872.1:g.27764C>A , LRG_121:g.27764C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*770C>A	ENSP00000514307.1:n.*770C>A
ENST00000525976.6:c.2421C>A	ENSP00000434831.2:p.Ile807=
ENST00000527481.3:c.2421C>A	ENSP00000466340.2:p.Ile807=
ENST00000529370.6:n.2752C>A
ENST00000529739.2:n.2835C>A
ENST00000530829.2:c.*1972C>A	ENSP00000436826.2:n.*1972C>A
ENST00000531836.6:c.2421C>A	ENSP00000436175.2:p.Ile807=
ENST00000533334.2:c.*463C>A	ENSP00000432320.2:n.*463C>A
ENST00000534228.2:n.2835C>A
ENST00000699354.1:n.523C>A
ENST00000699355.1:c.*481C>A	ENSP00000514328.1:n.*481C>A
ENST00000699356.1:n.2835C>A
ENST00000699357.1:n.2835C>A
ENST00000699358.1:c.2421C>A	ENSP00000514329.1:p.Ile807=
ENST00000699360.1:c.2421C>A	ENSP00000514331.1:p.Ile807=
ENST00000525621.6:c.2421C>A MANE Select	ENSP00000431885.1:p.Ile807=
ENST00000264818.10:c.2421C>A	ENSP00000264818.6:p.Ile807=
ENST00000524462.5:c.1866C>A	ENSP00000433203.1:p.Ile622=
ENST00000525621.5:c.2421C>A	ENSP00000431885.1:p.Ile807=
ENST00000529370.5:c.2421C>A	ENSP00000432728.1:p.Ile807=
ENST00000529412.1:n.93C>A
ENST00000533334.1:c.710C>A
NM_003331.4:c.2421C>A , LRG_121t1:c.2421C>A	NP_003322.3:p.Ile807=
XM_011528245.1:c.2421C>A	XP_011526547.1:p.Ile807=
XM_011528246.1:c.2124C>A	XP_011526548.1:p.Ile708=
XM_011528247.1:c.2124C>A	XP_011526549.1:p.Ile708=
XM_011528248.1:c.2421C>A	XP_011526550.1:p.Ile807=
XM_011528249.1:c.1095C>A	XP_011526551.1:p.Ile365=
XM_011528251.1:c.678C>A	XP_011526553.1:p.Ile226=
XM_011528246.3:c.2124C>A	XP_011526548.1:p.Ile708=
XM_011528249.2:c.1095C>A	XP_011526551.1:p.Ile365=
XR_001753750.1:n.2578C>A
XR_001753751.1:n.2578C>A
XR_002958353.1:n.2459C>A
NM_003331.5:c.2421C>A MANE Select	NP_003322.3:p.Ile807=
NM_001385197.1:c.2421C>A	NP_001372126.1:p.Ile807=
NM_001385198.1:c.2421C>A	NP_001372127.1:p.Ile807=
NM_001385199.1:c.2235C>A	NP_001372128.1:p.Ile745=
NM_001385200.1:c.2421C>A	NP_001372129.1:p.Ile807=
NM_001385201.1:c.2223C>A	NP_001372130.1:p.Ile741=
NM_001385202.1:c.2337C>A	NP_001372131.1:p.Ile779=
NM_001385203.1:c.2421C>A	NP_001372132.1:p.Ile807=
NM_001385204.1:c.2421C>A	NP_001372133.1:p.Ile807=
NM_001385205.1:c.2331C>A	NP_001372134.1:p.Ile777=
NM_001385206.1:c.2295C>A	NP_001372135.1:p.Ile765=
NM_001385207.1:c.2403C>A	NP_001372136.1:p.Ile801=