Canonical Allele Identifier: CA505371463

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463218T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352542T>C , CM000681.2:g.10352542T>C	GRCh38
NC_000019.9:g.10463218T>C , CM000681.1:g.10463218T>C	GRCh37
NC_000019.8:g.10324218T>C	NCBI36
NG_007872.1:g.33031A>G , LRG_121:g.33031A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1559A>G	ENSP00000514307.1:n.*1559A>G
ENST00000525976.6:c.3210A>G	ENSP00000434831.2:p.Pro1070=
ENST00000527481.3:c.3091A>G	ENSP00000466340.2:p.Arg1031Gly
ENST00000529370.6:n.4586A>G
ENST00000529739.2:n.4019A>G
ENST00000530829.2:c.*2761A>G	ENSP00000436826.2:n.*2761A>G
ENST00000531836.6:c.3210A>G	ENSP00000436175.2:p.Pro1070=
ENST00000533334.2:c.*1242+384A>G	ENSP00000432320.2:n.*1242+384A>G
ENST00000534228.2:n.5054+384A>G
ENST00000699354.1:n.1312A>G
ENST00000699355.1:c.*2710A>G	ENSP00000514328.1:n.*2710A>G
ENST00000699356.1:n.4019A>G
ENST00000699357.1:n.5064A>G
ENST00000699358.1:c.3200+384A>G	ENSP00000514329.1:n.3200+384A>G
ENST00000699359.1:c.384A>G
ENST00000699360.1:c.3168A>G	ENSP00000514331.1:p.Pro1056=
ENST00000699361.1:n.244A>G
ENST00000699362.1:c.106A>G	ENSP00000514332.1:p.Arg36Gly
ENST00000699363.1:c.106A>G	ENSP00000514333.1:p.Arg36Gly
ENST00000699364.1:n.210A>G
ENST00000699365.1:c.279A>G	ENSP00000514334.1:p.Pro93=
ENST00000699366.1:n.111+1272A>G
ENST00000699367.1:n.111+1272A>G
ENST00000699368.1:c.697A>G	ENSP00000514335.1:n.697A>G
ENST00000525621.6:c.3210A>G MANE Select	ENSP00000431885.1:p.Pro1070=
ENST00000264818.10:c.3210A>G	ENSP00000264818.6:p.Pro1070=
ENST00000524462.5:c.2655A>G	ENSP00000433203.1:p.Pro885=
ENST00000525621.5:c.3210A>G	ENSP00000431885.1:p.Pro1070=
ENST00000527481.2:c.387A>G
ENST00000529422.1:n.116+480A>G
ENST00000529739.1:c.279A>G	ENSP00000436155.1:p.Pro93=
ENST00000530220.1:n.331+384A>G
ENST00000530560.5:c.337+1500A>G	ENSP00000465291.1:n.337+1500A>G
ENST00000592137.1:n.364A>G
NM_003331.4:c.3210A>G , LRG_121t1:c.3210A>G	NP_003322.3:p.Pro1070=
XM_011528245.1:c.3210A>G	XP_011526547.1:p.Pro1070=
XM_011528246.1:c.2913A>G	XP_011526548.1:p.Pro971=
XM_011528247.1:c.2913A>G	XP_011526549.1:p.Pro971=
XM_011528248.1:c.3200+384A>G	XP_011526550.1:n.3200+384A>G
XM_011528249.1:c.1884A>G	XP_011526551.1:p.Pro628=
XM_011528251.1:c.1467A>G	XP_011526553.1:p.Pro489=
XM_011528246.3:c.2913A>G	XP_011526548.1:p.Pro971=
XM_011528249.2:c.1884A>G	XP_011526551.1:p.Pro628=
XR_001753750.1:n.3357+384A>G
XR_001753751.1:n.3762A>G
XR_002958353.1:n.4688A>G
NM_003331.5:c.3210A>G MANE Select	NP_003322.3:p.Pro1070=
NM_001385197.1:c.3210A>G	NP_001372126.1:p.Pro1070=
NM_001385198.1:c.3168+416A>G	NP_001372127.1:n.3168+416A>G
NM_001385199.1:c.3024A>G	NP_001372128.1:p.Pro1008=
NM_001385200.1:c.3207A>G	NP_001372129.1:p.Pro1069=
NM_001385201.1:c.3012A>G	NP_001372130.1:p.Pro1004=
NM_001385202.1:c.3126A>G	NP_001372131.1:p.Pro1042=
NM_001385203.1:c.3291A>G	NP_001372132.1:p.Pro1097=
NM_001385204.1:c.3420A>G	NP_001372133.1:p.Pro1140=
NM_001385205.1:c.3120A>G	NP_001372134.1:p.Pro1040=
NM_001385206.1:c.3084A>G	NP_001372135.1:p.Pro1028=
NM_001385207.1:c.3192A>G	NP_001372136.1:p.Pro1064=