Canonical Allele Identifier: CA403983198

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463156A>T (hg19) ; chr19:g.10352480A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352480A>T , CM000681.2:g.10352480A>T	GRCh38
NC_000019.9:g.10463156A>T , CM000681.1:g.10463156A>T	GRCh37
NC_000019.8:g.10324156A>T	NCBI36
NG_007872.1:g.33093T>A , LRG_121:g.33093T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1621T>A	ENSP00000514307.1:n.*1621T>A
ENST00000525976.6:c.3272T>A	ENSP00000434831.2:p.Leu1091Gln
ENST00000527481.3:c.*42T>A	ENSP00000466340.2:n.*42T>A
ENST00000529370.6:n.4648T>A
ENST00000529739.2:n.4081T>A
ENST00000530829.2:c.*2823T>A	ENSP00000436826.2:n.*2823T>A
ENST00000531836.6:c.3272T>A	ENSP00000436175.2:p.Leu1091Gln
ENST00000533334.2:c.*1242+446T>A	ENSP00000432320.2:n.*1242+446T>A
ENST00000534228.2:n.5054+446T>A
ENST00000699354.1:n.1374T>A
ENST00000699355.1:c.*2772T>A	ENSP00000514328.1:n.*2772T>A
ENST00000699356.1:n.4081T>A
ENST00000699357.1:n.5126T>A
ENST00000699358.1:c.3200+446T>A	ENSP00000514329.1:n.3200+446T>A
ENST00000699359.1:c.446T>A
ENST00000699360.1:c.3230T>A	ENSP00000514331.1:p.Leu1077Gln
ENST00000699361.1:n.306T>A
ENST00000699362.1:c.168T>A	ENSP00000514332.1:n.168T>A
ENST00000699363.1:c.168T>A	ENSP00000514333.1:n.168T>A
ENST00000699364.1:n.272T>A
ENST00000699365.1:c.341T>A	ENSP00000514334.1:p.Leu114Gln
ENST00000699366.1:n.111+1334T>A
ENST00000699367.1:n.112-1318T>A
ENST00000699368.1:c.759T>A	ENSP00000514335.1:n.759T>A
ENST00000525621.6:c.3272T>A MANE Select	ENSP00000431885.1:p.Leu1091Gln
ENST00000264818.10:c.3272T>A	ENSP00000264818.6:p.Leu1091Gln
ENST00000524462.5:c.2717T>A	ENSP00000433203.1:p.Leu906Gln
ENST00000525621.5:c.3272T>A	ENSP00000431885.1:p.Leu1091Gln
ENST00000525976.5:c.13T>A
ENST00000527481.2:c.449T>A
ENST00000529422.1:n.116+542T>A
ENST00000529739.1:c.341T>A	ENSP00000436155.1:p.Leu114Gln
ENST00000530220.1:n.331+446T>A
ENST00000530560.5:c.338-1512T>A	ENSP00000465291.1:n.338-1512T>A
ENST00000592137.1:n.426T>A
NM_003331.4:c.3272T>A , LRG_121t1:c.3272T>A	NP_003322.3:p.Leu1091Gln
XM_011528245.1:c.3272T>A	XP_011526547.1:p.Leu1091Gln
XM_011528246.1:c.2975T>A	XP_011526548.1:p.Leu992Gln
XM_011528247.1:c.2975T>A	XP_011526549.1:p.Leu992Gln
XM_011528248.1:c.3200+446T>A	XP_011526550.1:n.3200+446T>A
XM_011528249.1:c.1946T>A	XP_011526551.1:p.Leu649Gln
XM_011528251.1:c.1529T>A	XP_011526553.1:p.Leu510Gln
XM_011528246.3:c.2975T>A	XP_011526548.1:p.Leu992Gln
XM_011528249.2:c.1946T>A	XP_011526551.1:p.Leu649Gln
XR_001753750.1:n.3357+446T>A
XR_001753751.1:n.3824T>A
XR_002958353.1:n.4750T>A
NM_003331.5:c.3272T>A MANE Select	NP_003322.3:p.Leu1091Gln
NM_001385197.1:c.3272T>A	NP_001372126.1:p.Leu1091Gln
NM_001385198.1:c.3168+478T>A	NP_001372127.1:n.3168+478T>A
NM_001385199.1:c.3086T>A	NP_001372128.1:p.Leu1029Gln
NM_001385200.1:c.3269T>A	NP_001372129.1:p.Leu1090Gln
NM_001385201.1:c.3074T>A	NP_001372130.1:p.Leu1025Gln
NM_001385202.1:c.3188T>A	NP_001372131.1:p.Leu1063Gln
NM_001385203.1:c.3353T>A	NP_001372132.1:p.Leu1118Gln
NM_001385204.1:c.3482T>A	NP_001372133.1:p.Leu1161Gln
NM_001385205.1:c.3182T>A	NP_001372134.1:p.Leu1061Gln
NM_001385206.1:c.3146T>A	NP_001372135.1:p.Leu1049Gln
NM_001385207.1:c.3254T>A	NP_001372136.1:p.Leu1085Gln