Canonical Allele Identifier: CA403983357

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463226A>T (hg19) ; chr19:g.10352550A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352550A>T , CM000681.2:g.10352550A>T	GRCh38
NC_000019.9:g.10463226A>T , CM000681.1:g.10463226A>T	GRCh37
NC_000019.8:g.10324226A>T	NCBI36
NG_007872.1:g.33023T>A , LRG_121:g.33023T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1551T>A	ENSP00000514307.1:n.*1551T>A
ENST00000525976.6:c.3202T>A	ENSP00000434831.2:p.Tyr1068Asn
ENST00000527481.3:c.3083T>A	ENSP00000466340.2:p.Val1028Glu
ENST00000529370.6:n.4578T>A
ENST00000529739.2:n.4011T>A
ENST00000530829.2:c.*2753T>A	ENSP00000436826.2:n.*2753T>A
ENST00000531836.6:c.3202T>A	ENSP00000436175.2:p.Tyr1068Asn
ENST00000533334.2:c.*1242+376T>A	ENSP00000432320.2:n.*1242+376T>A
ENST00000534228.2:n.5054+376T>A
ENST00000699354.1:n.1304T>A
ENST00000699355.1:c.*2702T>A	ENSP00000514328.1:n.*2702T>A
ENST00000699356.1:n.4011T>A
ENST00000699357.1:n.5056T>A
ENST00000699358.1:c.3200+376T>A	ENSP00000514329.1:n.3200+376T>A
ENST00000699359.1:c.376T>A
ENST00000699360.1:c.3160T>A	ENSP00000514331.1:p.Tyr1054Asn
ENST00000699361.1:n.236T>A
ENST00000699362.1:c.98T>A	ENSP00000514332.1:p.Val33Glu
ENST00000699363.1:c.98T>A	ENSP00000514333.1:p.Val33Glu
ENST00000699364.1:n.202T>A
ENST00000699365.1:c.271T>A	ENSP00000514334.1:p.Tyr91Asn
ENST00000699366.1:n.111+1264T>A
ENST00000699367.1:n.111+1264T>A
ENST00000699368.1:c.689T>A	ENSP00000514335.1:n.689T>A
ENST00000525621.6:c.3202T>A MANE Select	ENSP00000431885.1:p.Tyr1068Asn
ENST00000264818.10:c.3202T>A	ENSP00000264818.6:p.Tyr1068Asn
ENST00000524462.5:c.2647T>A	ENSP00000433203.1:p.Tyr883Asn
ENST00000525621.5:c.3202T>A	ENSP00000431885.1:p.Tyr1068Asn
ENST00000527481.2:c.379T>A
ENST00000529422.1:n.116+472T>A
ENST00000529739.1:c.271T>A	ENSP00000436155.1:p.Tyr91Asn
ENST00000530220.1:n.331+376T>A
ENST00000530560.5:c.337+1492T>A	ENSP00000465291.1:n.337+1492T>A
ENST00000592137.1:n.356T>A
NM_003331.4:c.3202T>A , LRG_121t1:c.3202T>A	NP_003322.3:p.Tyr1068Asn
XM_011528245.1:c.3202T>A	XP_011526547.1:p.Tyr1068Asn
XM_011528246.1:c.2905T>A	XP_011526548.1:p.Tyr969Asn
XM_011528247.1:c.2905T>A	XP_011526549.1:p.Tyr969Asn
XM_011528248.1:c.3200+376T>A	XP_011526550.1:n.3200+376T>A
XM_011528249.1:c.1876T>A	XP_011526551.1:p.Tyr626Asn
XM_011528251.1:c.1459T>A	XP_011526553.1:p.Tyr487Asn
XM_011528246.3:c.2905T>A	XP_011526548.1:p.Tyr969Asn
XM_011528249.2:c.1876T>A	XP_011526551.1:p.Tyr626Asn
XR_001753750.1:n.3357+376T>A
XR_001753751.1:n.3754T>A
XR_002958353.1:n.4680T>A
NM_003331.5:c.3202T>A MANE Select	NP_003322.3:p.Tyr1068Asn
NM_001385197.1:c.3202T>A	NP_001372126.1:p.Tyr1068Asn
NM_001385198.1:c.3168+408T>A	NP_001372127.1:n.3168+408T>A
NM_001385199.1:c.3016T>A	NP_001372128.1:p.Tyr1006Asn
NM_001385200.1:c.3199T>A	NP_001372129.1:p.Tyr1067Asn
NM_001385201.1:c.3004T>A	NP_001372130.1:p.Tyr1002Asn
NM_001385202.1:c.3118T>A	NP_001372131.1:p.Tyr1040Asn
NM_001385203.1:c.3283T>A	NP_001372132.1:p.Tyr1095Asn
NM_001385204.1:c.3412T>A	NP_001372133.1:p.Tyr1138Asn
NM_001385205.1:c.3112T>A	NP_001372134.1:p.Tyr1038Asn
NM_001385206.1:c.3076T>A	NP_001372135.1:p.Tyr1026Asn
NM_001385207.1:c.3184T>A	NP_001372136.1:p.Tyr1062Asn