Canonical Allele Identifier: CA403982877

Gene: TYK2

Linked Data

• gnomAD v4: 19-10352442-G-T
• MyVariant Identifiers: chr19:g.10463118G>T (hg19) ; chr19:g.10352442G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352442G>T , CM000681.2:g.10352442G>T	GRCh38
NC_000019.9:g.10463118G>T , CM000681.1:g.10463118G>T	GRCh37
NC_000019.8:g.10324118G>T	NCBI36
NG_007872.1:g.33131C>A , LRG_121:g.33131C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.*1659C>A	ENSP00000514307.1:n.*1659C>A
ENST00000525976.6:c.3310C>A	ENSP00000434831.2:p.Pro1104Thr
ENST00000527481.3:c.*80C>A	ENSP00000466340.2:n.*80C>A
ENST00000529370.6:n.4686C>A
ENST00000529739.2:n.4119C>A
ENST00000530829.2:c.*2861C>A	ENSP00000436826.2:n.*2861C>A
ENST00000531836.6:c.3310C>A	ENSP00000436175.2:p.Pro1104Thr
ENST00000533334.2:c.*1242+484C>A	ENSP00000432320.2:n.*1242+484C>A
ENST00000534228.2:n.5054+484C>A
ENST00000699354.1:n.1412C>A
ENST00000699355.1:c.*2810C>A	ENSP00000514328.1:n.*2810C>A
ENST00000699356.1:n.4119C>A
ENST00000699357.1:n.5164C>A
ENST00000699358.1:c.3200+484C>A	ENSP00000514329.1:n.3200+484C>A
ENST00000699359.1:c.484C>A
ENST00000699360.1:c.3268C>A	ENSP00000514331.1:p.Pro1090Thr
ENST00000699361.1:n.344C>A
ENST00000699362.1:c.206C>A	ENSP00000514332.1:n.206C>A
ENST00000699363.1:c.206C>A	ENSP00000514333.1:n.206C>A
ENST00000699364.1:n.310C>A
ENST00000699365.1:c.379C>A	ENSP00000514334.1:p.Pro127Thr
ENST00000699366.1:n.111+1372C>A
ENST00000699367.1:n.112-1280C>A
ENST00000699368.1:c.797C>A	ENSP00000514335.1:n.797C>A
ENST00000525621.6:c.3310C>A MANE Select	ENSP00000431885.1:p.Pro1104Thr
ENST00000264818.10:c.3310C>A	ENSP00000264818.6:p.Pro1104Thr
ENST00000524462.5:c.2755C>A	ENSP00000433203.1:p.Pro919Thr
ENST00000525621.5:c.3310C>A	ENSP00000431885.1:p.Pro1104Thr
ENST00000525976.5:c.51C>A
ENST00000527481.2:c.487C>A
ENST00000529422.1:n.116+580C>A
ENST00000529739.1:c.379C>A	ENSP00000436155.1:p.Pro127Thr
ENST00000530220.1:n.331+484C>A
ENST00000530560.5:c.338-1474C>A	ENSP00000465291.1:n.338-1474C>A
ENST00000592137.1:n.464C>A
NM_003331.4:c.3310C>A , LRG_121t1:c.3310C>A	NP_003322.3:p.Pro1104Thr
XM_011528245.1:c.3310C>A	XP_011526547.1:p.Pro1104Thr
XM_011528246.1:c.3013C>A	XP_011526548.1:p.Pro1005Thr
XM_011528247.1:c.3013C>A	XP_011526549.1:p.Pro1005Thr
XM_011528248.1:c.3200+484C>A	XP_011526550.1:n.3200+484C>A
XM_011528249.1:c.1984C>A	XP_011526551.1:p.Pro662Thr
XM_011528251.1:c.1567C>A	XP_011526553.1:p.Pro523Thr
XM_011528246.3:c.3013C>A	XP_011526548.1:p.Pro1005Thr
XM_011528249.2:c.1984C>A	XP_011526551.1:p.Pro662Thr
XR_001753750.1:n.3357+484C>A
XR_001753751.1:n.3862C>A
XR_002958353.1:n.4788C>A
NM_003331.5:c.3310C>A MANE Select	NP_003322.3:p.Pro1104Thr
NM_001385197.1:c.3310C>A	NP_001372126.1:p.Pro1104Thr
NM_001385198.1:c.3168+516C>A	NP_001372127.1:n.3168+516C>A
NM_001385199.1:c.3124C>A	NP_001372128.1:p.Pro1042Thr
NM_001385200.1:c.3307C>A	NP_001372129.1:p.Pro1103Thr
NM_001385201.1:c.3112C>A	NP_001372130.1:p.Pro1038Thr
NM_001385202.1:c.3226C>A	NP_001372131.1:p.Pro1076Thr
NM_001385203.1:c.3391C>A	NP_001372132.1:p.Pro1131Thr
NM_001385204.1:c.3520C>A	NP_001372133.1:p.Pro1174Thr
NM_001385205.1:c.3220C>A	NP_001372134.1:p.Pro1074Thr
NM_001385206.1:c.3184C>A	NP_001372135.1:p.Pro1062Thr
NM_001385207.1:c.3292C>A	NP_001372136.1:p.Pro1098Thr