Canonical Allele Identifier: CA403983300

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463202A>T (hg19) ; chr19:g.10352526A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352526A>T , CM000681.2:g.10352526A>T	GRCh38
NC_000019.9:g.10463202A>T , CM000681.1:g.10463202A>T	GRCh37
NC_000019.8:g.10324202A>T	NCBI36
NG_007872.1:g.33047T>A , LRG_121:g.33047T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1575T>A	ENSP00000514307.1:n.*1575T>A
ENST00000525976.6:c.3226T>A	ENSP00000434831.2:p.Tyr1076Asn
ENST00000527481.3:c.3107T>A	ENSP00000466340.2:p.Val1036Glu
ENST00000529370.6:n.4602T>A
ENST00000529739.2:n.4035T>A
ENST00000530829.2:c.*2777T>A	ENSP00000436826.2:n.*2777T>A
ENST00000531836.6:c.3226T>A	ENSP00000436175.2:p.Tyr1076Asn
ENST00000533334.2:c.*1242+400T>A	ENSP00000432320.2:n.*1242+400T>A
ENST00000534228.2:n.5054+400T>A
ENST00000699354.1:n.1328T>A
ENST00000699355.1:c.*2726T>A	ENSP00000514328.1:n.*2726T>A
ENST00000699356.1:n.4035T>A
ENST00000699357.1:n.5080T>A
ENST00000699358.1:c.3200+400T>A	ENSP00000514329.1:n.3200+400T>A
ENST00000699359.1:c.400T>A
ENST00000699360.1:c.3184T>A	ENSP00000514331.1:p.Tyr1062Asn
ENST00000699361.1:n.260T>A
ENST00000699362.1:c.122T>A	ENSP00000514332.1:p.Val41Glu
ENST00000699363.1:c.122T>A	ENSP00000514333.1:p.Val41Glu
ENST00000699364.1:n.226T>A
ENST00000699365.1:c.295T>A	ENSP00000514334.1:p.Tyr99Asn
ENST00000699366.1:n.111+1288T>A
ENST00000699367.1:n.111+1288T>A
ENST00000699368.1:c.713T>A	ENSP00000514335.1:n.713T>A
ENST00000525621.6:c.3226T>A MANE Select	ENSP00000431885.1:p.Tyr1076Asn
ENST00000264818.10:c.3226T>A	ENSP00000264818.6:p.Tyr1076Asn
ENST00000524462.5:c.2671T>A	ENSP00000433203.1:p.Tyr891Asn
ENST00000525621.5:c.3226T>A	ENSP00000431885.1:p.Tyr1076Asn
ENST00000527481.2:c.403T>A
ENST00000529422.1:n.116+496T>A
ENST00000529739.1:c.295T>A	ENSP00000436155.1:p.Tyr99Asn
ENST00000530220.1:n.331+400T>A
ENST00000530560.5:c.337+1516T>A	ENSP00000465291.1:n.337+1516T>A
ENST00000592137.1:n.380T>A
NM_003331.4:c.3226T>A , LRG_121t1:c.3226T>A	NP_003322.3:p.Tyr1076Asn
XM_011528245.1:c.3226T>A	XP_011526547.1:p.Tyr1076Asn
XM_011528246.1:c.2929T>A	XP_011526548.1:p.Tyr977Asn
XM_011528247.1:c.2929T>A	XP_011526549.1:p.Tyr977Asn
XM_011528248.1:c.3200+400T>A	XP_011526550.1:n.3200+400T>A
XM_011528249.1:c.1900T>A	XP_011526551.1:p.Tyr634Asn
XM_011528251.1:c.1483T>A	XP_011526553.1:p.Tyr495Asn
XM_011528246.3:c.2929T>A	XP_011526548.1:p.Tyr977Asn
XM_011528249.2:c.1900T>A	XP_011526551.1:p.Tyr634Asn
XR_001753750.1:n.3357+400T>A
XR_001753751.1:n.3778T>A
XR_002958353.1:n.4704T>A
NM_003331.5:c.3226T>A MANE Select	NP_003322.3:p.Tyr1076Asn
NM_001385197.1:c.3226T>A	NP_001372126.1:p.Tyr1076Asn
NM_001385198.1:c.3168+432T>A	NP_001372127.1:n.3168+432T>A
NM_001385199.1:c.3040T>A	NP_001372128.1:p.Tyr1014Asn
NM_001385200.1:c.3223T>A	NP_001372129.1:p.Tyr1075Asn
NM_001385201.1:c.3028T>A	NP_001372130.1:p.Tyr1010Asn
NM_001385202.1:c.3142T>A	NP_001372131.1:p.Tyr1048Asn
NM_001385203.1:c.3307T>A	NP_001372132.1:p.Tyr1103Asn
NM_001385204.1:c.3436T>A	NP_001372133.1:p.Tyr1146Asn
NM_001385205.1:c.3136T>A	NP_001372134.1:p.Tyr1046Asn
NM_001385206.1:c.3100T>A	NP_001372135.1:p.Tyr1034Asn
NM_001385207.1:c.3208T>A	NP_001372136.1:p.Tyr1070Asn