Canonical Allele Identifier: CA505476480

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10468701G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10358025G>T , CM000681.2:g.10358025G>T	GRCh38
NC_000019.9:g.10468701G>T , CM000681.1:g.10468701G>T	GRCh37
NC_000019.8:g.10329701G>T	NCBI36
NG_007872.1:g.27548C>A , LRG_121:g.27548C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*638C>A	ENSP00000514307.1:n.*638C>A
ENST00000525976.6:c.2289C>A	ENSP00000434831.2:p.Gly763=
ENST00000527481.3:c.2289C>A	ENSP00000466340.2:p.Gly763=
ENST00000529370.6:n.2620C>A
ENST00000529739.2:n.2703C>A
ENST00000530829.2:c.*1840C>A	ENSP00000436826.2:n.*1840C>A
ENST00000531836.6:c.2289C>A	ENSP00000436175.2:p.Gly763=
ENST00000533334.2:c.*331C>A	ENSP00000432320.2:n.*331C>A
ENST00000534228.2:n.2703C>A
ENST00000699354.1:n.391C>A
ENST00000699355.1:c.*349C>A	ENSP00000514328.1:n.*349C>A
ENST00000699356.1:n.2703C>A
ENST00000699357.1:n.2703C>A
ENST00000699358.1:c.2289C>A	ENSP00000514329.1:p.Gly763=
ENST00000699360.1:c.2289C>A	ENSP00000514331.1:p.Gly763=
ENST00000525621.6:c.2289C>A MANE Select	ENSP00000431885.1:p.Gly763=
ENST00000264818.10:c.2289C>A	ENSP00000264818.6:p.Gly763=
ENST00000524462.5:c.1734C>A	ENSP00000433203.1:p.Gly578=
ENST00000525621.5:c.2289C>A	ENSP00000431885.1:p.Gly763=
ENST00000529370.5:c.2289C>A	ENSP00000432728.1:p.Gly763=
ENST00000533334.1:c.578C>A
NM_003331.4:c.2289C>A , LRG_121t1:c.2289C>A	NP_003322.3:p.Gly763=
XM_011528245.1:c.2289C>A	XP_011526547.1:p.Gly763=
XM_011528246.1:c.1992C>A	XP_011526548.1:p.Gly664=
XM_011528247.1:c.1992C>A	XP_011526549.1:p.Gly664=
XM_011528248.1:c.2289C>A	XP_011526550.1:p.Gly763=
XM_011528249.1:c.963C>A	XP_011526551.1:p.Gly321=
XM_011528251.1:c.546C>A	XP_011526553.1:p.Gly182=
XM_011528246.3:c.1992C>A	XP_011526548.1:p.Gly664=
XM_011528249.2:c.963C>A	XP_011526551.1:p.Gly321=
XR_001753750.1:n.2446C>A
XR_001753751.1:n.2446C>A
XR_001753752.1:n.2558C>A
XR_002958353.1:n.2327C>A
NM_003331.5:c.2289C>A MANE Select	NP_003322.3:p.Gly763=
NM_001385197.1:c.2289C>A	NP_001372126.1:p.Gly763=
NM_001385198.1:c.2289C>A	NP_001372127.1:p.Gly763=
NM_001385199.1:c.2103C>A	NP_001372128.1:p.Gly701=
NM_001385200.1:c.2289C>A	NP_001372129.1:p.Gly763=
NM_001385201.1:c.2091C>A	NP_001372130.1:p.Gly697=
NM_001385202.1:c.2205C>A	NP_001372131.1:p.Gly735=
NM_001385203.1:c.2289C>A	NP_001372132.1:p.Gly763=
NM_001385204.1:c.2289C>A	NP_001372133.1:p.Gly763=
NM_001385205.1:c.2199C>A	NP_001372134.1:p.Gly733=
NM_001385206.1:c.2163C>A	NP_001372135.1:p.Gly721=
NM_001385207.1:c.2271C>A	NP_001372136.1:p.Gly757=