Canonical Allele Identifier: CA403983262

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463187C>G (hg19) ; chr19:g.10352511C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352511C>G , CM000681.2:g.10352511C>G	GRCh38
NC_000019.9:g.10463187C>G , CM000681.1:g.10463187C>G	GRCh37
NC_000019.8:g.10324187C>G	NCBI36
NG_007872.1:g.33062G>C , LRG_121:g.33062G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1590G>C	ENSP00000514307.1:n.*1590G>C
ENST00000525976.6:c.3241G>C	ENSP00000434831.2:p.Ala1081Pro
ENST00000527481.3:c.*11G>C	ENSP00000466340.2:n.*11G>C
ENST00000529370.6:n.4617G>C
ENST00000529739.2:n.4050G>C
ENST00000530829.2:c.*2792G>C	ENSP00000436826.2:n.*2792G>C
ENST00000531836.6:c.3241G>C	ENSP00000436175.2:p.Ala1081Pro
ENST00000533334.2:c.*1242+415G>C	ENSP00000432320.2:n.*1242+415G>C
ENST00000534228.2:n.5054+415G>C
ENST00000699354.1:n.1343G>C
ENST00000699355.1:c.*2741G>C	ENSP00000514328.1:n.*2741G>C
ENST00000699356.1:n.4050G>C
ENST00000699357.1:n.5095G>C
ENST00000699358.1:c.3200+415G>C	ENSP00000514329.1:n.3200+415G>C
ENST00000699359.1:c.415G>C
ENST00000699360.1:c.3199G>C	ENSP00000514331.1:p.Ala1067Pro
ENST00000699361.1:n.275G>C
ENST00000699362.1:c.137G>C	ENSP00000514332.1:n.137G>C
ENST00000699363.1:c.137G>C	ENSP00000514333.1:n.137G>C
ENST00000699364.1:n.241G>C
ENST00000699365.1:c.310G>C	ENSP00000514334.1:p.Ala104Pro
ENST00000699366.1:n.111+1303G>C
ENST00000699367.1:n.111+1303G>C
ENST00000699368.1:c.728G>C	ENSP00000514335.1:n.728G>C
ENST00000525621.6:c.3241G>C MANE Select	ENSP00000431885.1:p.Ala1081Pro
ENST00000264818.10:c.3241G>C	ENSP00000264818.6:p.Ala1081Pro
ENST00000524462.5:c.2686G>C	ENSP00000433203.1:p.Ala896Pro
ENST00000525621.5:c.3241G>C	ENSP00000431885.1:p.Ala1081Pro
ENST00000527481.2:c.418G>C
ENST00000529422.1:n.116+511G>C
ENST00000529739.1:c.310G>C	ENSP00000436155.1:p.Ala104Pro
ENST00000530220.1:n.331+415G>C
ENST00000530560.5:c.337+1531G>C	ENSP00000465291.1:n.337+1531G>C
ENST00000592137.1:n.395G>C
NM_003331.4:c.3241G>C , LRG_121t1:c.3241G>C	NP_003322.3:p.Ala1081Pro
XM_011528245.1:c.3241G>C	XP_011526547.1:p.Ala1081Pro
XM_011528246.1:c.2944G>C	XP_011526548.1:p.Ala982Pro
XM_011528247.1:c.2944G>C	XP_011526549.1:p.Ala982Pro
XM_011528248.1:c.3200+415G>C	XP_011526550.1:n.3200+415G>C
XM_011528249.1:c.1915G>C	XP_011526551.1:p.Ala639Pro
XM_011528251.1:c.1498G>C	XP_011526553.1:p.Ala500Pro
XM_011528246.3:c.2944G>C	XP_011526548.1:p.Ala982Pro
XM_011528249.2:c.1915G>C	XP_011526551.1:p.Ala639Pro
XR_001753750.1:n.3357+415G>C
XR_001753751.1:n.3793G>C
XR_002958353.1:n.4719G>C
NM_003331.5:c.3241G>C MANE Select	NP_003322.3:p.Ala1081Pro
NM_001385197.1:c.3241G>C	NP_001372126.1:p.Ala1081Pro
NM_001385198.1:c.3168+447G>C	NP_001372127.1:n.3168+447G>C
NM_001385199.1:c.3055G>C	NP_001372128.1:p.Ala1019Pro
NM_001385200.1:c.3238G>C	NP_001372129.1:p.Ala1080Pro
NM_001385201.1:c.3043G>C	NP_001372130.1:p.Ala1015Pro
NM_001385202.1:c.3157G>C	NP_001372131.1:p.Ala1053Pro
NM_001385203.1:c.3322G>C	NP_001372132.1:p.Ala1108Pro
NM_001385204.1:c.3451G>C	NP_001372133.1:p.Ala1151Pro
NM_001385205.1:c.3151G>C	NP_001372134.1:p.Ala1051Pro
NM_001385206.1:c.3115G>C	NP_001372135.1:p.Ala1039Pro
NM_001385207.1:c.3223G>C	NP_001372136.1:p.Ala1075Pro