Canonical Allele Identifier: CA403988260

Gene: TYK2

Linked Data

• gnomAD v4: 19-10354125-G-T
• MyVariant Identifiers: chr19:g.10464801G>T (hg19) ; chr19:g.10354125G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354125G>T , CM000681.2:g.10354125G>T	GRCh38
NC_000019.9:g.10464801G>T , CM000681.1:g.10464801G>T	GRCh37
NC_000019.8:g.10325801G>T	NCBI36
NG_007872.1:g.31448C>A , LRG_121:g.31448C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1174C>A	ENSP00000514307.1:n.*1174C>A
ENST00000525976.6:c.2825C>A	ENSP00000434831.2:p.Ser942Ter
ENST00000527481.3:c.2825C>A	ENSP00000466340.2:p.Ser942Ter
ENST00000529370.6:n.4201C>A
ENST00000529739.2:n.3239C>A
ENST00000530829.2:c.*2376C>A	ENSP00000436826.2:n.*2376C>A
ENST00000531836.6:c.2825C>A	ENSP00000436175.2:p.Ser942Ter
ENST00000533334.2:c.*867C>A	ENSP00000432320.2:n.*867C>A
ENST00000534228.2:n.4284C>A
ENST00000699354.1:n.927C>A
ENST00000699355.1:c.*1930C>A	ENSP00000514328.1:n.*1930C>A
ENST00000699356.1:n.3239C>A
ENST00000699357.1:n.4284C>A
ENST00000699358.1:c.2825C>A	ENSP00000514329.1:p.Ser942Ter
ENST00000699359.1:c.31C>A
ENST00000699360.1:c.2825C>A	ENSP00000514331.1:p.Ser942Ter
ENST00000699368.1:c.29C>A	ENSP00000514335.1:p.Ser10Ter
ENST00000525621.6:c.2825C>A MANE Select	ENSP00000431885.1:p.Ser942Ter
ENST00000264818.10:c.2825C>A	ENSP00000264818.6:p.Ser942Ter
ENST00000524462.5:c.2270C>A	ENSP00000433203.1:p.Ser757Ter
ENST00000525621.5:c.2825C>A	ENSP00000431885.1:p.Ser942Ter
ENST00000527481.2:c.121C>A
ENST00000529412.1:n.497C>A
ENST00000530560.5:c.254C>A	ENSP00000465291.1:p.Ser85Ter
NM_003331.4:c.2825C>A , LRG_121t1:c.2825C>A	NP_003322.3:p.Ser942Ter
XM_011528245.1:c.2825C>A	XP_011526547.1:p.Ser942Ter
XM_011528246.1:c.2528C>A	XP_011526548.1:p.Ser843Ter
XM_011528247.1:c.2528C>A	XP_011526549.1:p.Ser843Ter
XM_011528248.1:c.2825C>A	XP_011526550.1:p.Ser942Ter
XM_011528249.1:c.1499C>A	XP_011526551.1:p.Ser500Ter
XM_011528251.1:c.1082C>A	XP_011526553.1:p.Ser361Ter
XM_011528246.3:c.2528C>A	XP_011526548.1:p.Ser843Ter
XM_011528249.2:c.1499C>A	XP_011526551.1:p.Ser500Ter
XR_001753750.1:n.2982C>A
XR_001753751.1:n.2982C>A
XR_002958353.1:n.3908C>A
NM_003331.5:c.2825C>A MANE Select	NP_003322.3:p.Ser942Ter
NM_001385197.1:c.2825C>A	NP_001372126.1:p.Ser942Ter
NM_001385198.1:c.2825C>A	NP_001372127.1:p.Ser942Ter
NM_001385199.1:c.2639C>A	NP_001372128.1:p.Ser880Ter
NM_001385200.1:c.2822C>A	NP_001372129.1:p.Ser941Ter
NM_001385201.1:c.2627C>A	NP_001372130.1:p.Ser876Ter
NM_001385202.1:c.2741C>A	NP_001372131.1:p.Ser914Ter
NM_001385203.1:c.2906C>A	NP_001372132.1:p.Ser969Ter
NM_001385204.1:c.3035C>A	NP_001372133.1:p.Ser1012Ter
NM_001385205.1:c.2735C>A	NP_001372134.1:p.Ser912Ter
NM_001385206.1:c.2699C>A	NP_001372135.1:p.Ser900Ter
NM_001385207.1:c.2807C>A	NP_001372136.1:p.Ser936Ter