Canonical Allele Identifier: CA403983028

Gene: TYK2

Linked Data

• gnomAD v4: 19-10352456-T-A
• MyVariant Identifiers: chr19:g.10463132T>A (hg19) ; chr19:g.10352456T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352456T>A , CM000681.2:g.10352456T>A	GRCh38
NC_000019.9:g.10463132T>A , CM000681.1:g.10463132T>A	GRCh37
NC_000019.8:g.10324132T>A	NCBI36
NG_007872.1:g.33117A>T , LRG_121:g.33117A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1645A>T	ENSP00000514307.1:n.*1645A>T
ENST00000525976.6:c.3296A>T	ENSP00000434831.2:p.Asp1099Val
ENST00000527481.3:c.*66A>T	ENSP00000466340.2:n.*66A>T
ENST00000529370.6:n.4672A>T
ENST00000529739.2:n.4105A>T
ENST00000530829.2:c.*2847A>T	ENSP00000436826.2:n.*2847A>T
ENST00000531836.6:c.3296A>T	ENSP00000436175.2:p.Asp1099Val
ENST00000533334.2:c.*1242+470A>T	ENSP00000432320.2:n.*1242+470A>T
ENST00000534228.2:n.5054+470A>T
ENST00000699354.1:n.1398A>T
ENST00000699355.1:c.*2796A>T	ENSP00000514328.1:n.*2796A>T
ENST00000699356.1:n.4105A>T
ENST00000699357.1:n.5150A>T
ENST00000699358.1:c.3200+470A>T	ENSP00000514329.1:n.3200+470A>T
ENST00000699359.1:c.470A>T
ENST00000699360.1:c.3254A>T	ENSP00000514331.1:p.Asp1085Val
ENST00000699361.1:n.330A>T
ENST00000699362.1:c.192A>T	ENSP00000514332.1:n.192A>T
ENST00000699363.1:c.192A>T	ENSP00000514333.1:n.192A>T
ENST00000699364.1:n.296A>T
ENST00000699365.1:c.365A>T	ENSP00000514334.1:p.Asp122Val
ENST00000699366.1:n.111+1358A>T
ENST00000699367.1:n.112-1294A>T
ENST00000699368.1:c.783A>T	ENSP00000514335.1:n.783A>T
ENST00000525621.6:c.3296A>T MANE Select	ENSP00000431885.1:p.Asp1099Val
ENST00000264818.10:c.3296A>T	ENSP00000264818.6:p.Asp1099Val
ENST00000524462.5:c.2741A>T	ENSP00000433203.1:p.Asp914Val
ENST00000525621.5:c.3296A>T	ENSP00000431885.1:p.Asp1099Val
ENST00000525976.5:c.37A>T
ENST00000527481.2:c.473A>T
ENST00000529422.1:n.116+566A>T
ENST00000529739.1:c.365A>T	ENSP00000436155.1:p.Asp122Val
ENST00000530220.1:n.331+470A>T
ENST00000530560.5:c.338-1488A>T	ENSP00000465291.1:n.338-1488A>T
ENST00000592137.1:n.450A>T
NM_003331.4:c.3296A>T , LRG_121t1:c.3296A>T	NP_003322.3:p.Asp1099Val
XM_011528245.1:c.3296A>T	XP_011526547.1:p.Asp1099Val
XM_011528246.1:c.2999A>T	XP_011526548.1:p.Asp1000Val
XM_011528247.1:c.2999A>T	XP_011526549.1:p.Asp1000Val
XM_011528248.1:c.3200+470A>T	XP_011526550.1:n.3200+470A>T
XM_011528249.1:c.1970A>T	XP_011526551.1:p.Asp657Val
XM_011528251.1:c.1553A>T	XP_011526553.1:p.Asp518Val
XM_011528246.3:c.2999A>T	XP_011526548.1:p.Asp1000Val
XM_011528249.2:c.1970A>T	XP_011526551.1:p.Asp657Val
XR_001753750.1:n.3357+470A>T
XR_001753751.1:n.3848A>T
XR_002958353.1:n.4774A>T
NM_003331.5:c.3296A>T MANE Select	NP_003322.3:p.Asp1099Val
NM_001385197.1:c.3296A>T	NP_001372126.1:p.Asp1099Val
NM_001385198.1:c.3168+502A>T	NP_001372127.1:n.3168+502A>T
NM_001385199.1:c.3110A>T	NP_001372128.1:p.Asp1037Val
NM_001385200.1:c.3293A>T	NP_001372129.1:p.Asp1098Val
NM_001385201.1:c.3098A>T	NP_001372130.1:p.Asp1033Val
NM_001385202.1:c.3212A>T	NP_001372131.1:p.Asp1071Val
NM_001385203.1:c.3377A>T	NP_001372132.1:p.Asp1126Val
NM_001385204.1:c.3506A>T	NP_001372133.1:p.Asp1169Val
NM_001385205.1:c.3206A>T	NP_001372134.1:p.Asp1069Val
NM_001385206.1:c.3170A>T	NP_001372135.1:p.Asp1057Val
NM_001385207.1:c.3278A>T	NP_001372136.1:p.Asp1093Val