Canonical Allele Identifier: CA403982978

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463126C>T (hg19) ; chr19:g.10352450C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352450C>T , CM000681.2:g.10352450C>T	GRCh38
NC_000019.9:g.10463126C>T , CM000681.1:g.10463126C>T	GRCh37
NC_000019.8:g.10324126C>T	NCBI36
NG_007872.1:g.33123G>A , LRG_121:g.33123G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.*1651G>A	ENSP00000514307.1:n.*1651G>A
ENST00000525976.6:c.3302G>A	ENSP00000434831.2:p.Ser1101Asn
ENST00000527481.3:c.*72G>A	ENSP00000466340.2:n.*72G>A
ENST00000529370.6:n.4678G>A
ENST00000529739.2:n.4111G>A
ENST00000530829.2:c.*2853G>A	ENSP00000436826.2:n.*2853G>A
ENST00000531836.6:c.3302G>A	ENSP00000436175.2:p.Ser1101Asn
ENST00000533334.2:c.*1242+476G>A	ENSP00000432320.2:n.*1242+476G>A
ENST00000534228.2:n.5054+476G>A
ENST00000699354.1:n.1404G>A
ENST00000699355.1:c.*2802G>A	ENSP00000514328.1:n.*2802G>A
ENST00000699356.1:n.4111G>A
ENST00000699357.1:n.5156G>A
ENST00000699358.1:c.3200+476G>A	ENSP00000514329.1:n.3200+476G>A
ENST00000699359.1:c.476G>A
ENST00000699360.1:c.3260G>A	ENSP00000514331.1:p.Ser1087Asn
ENST00000699361.1:n.336G>A
ENST00000699362.1:c.198G>A	ENSP00000514332.1:n.198G>A
ENST00000699363.1:c.198G>A	ENSP00000514333.1:n.198G>A
ENST00000699364.1:n.302G>A
ENST00000699365.1:c.371G>A	ENSP00000514334.1:p.Ser124Asn
ENST00000699366.1:n.111+1364G>A
ENST00000699367.1:n.112-1288G>A
ENST00000699368.1:c.789G>A	ENSP00000514335.1:n.789G>A
ENST00000525621.6:c.3302G>A MANE Select	ENSP00000431885.1:p.Ser1101Asn
ENST00000264818.10:c.3302G>A	ENSP00000264818.6:p.Ser1101Asn
ENST00000524462.5:c.2747G>A	ENSP00000433203.1:p.Ser916Asn
ENST00000525621.5:c.3302G>A	ENSP00000431885.1:p.Ser1101Asn
ENST00000525976.5:c.43G>A
ENST00000527481.2:c.479G>A
ENST00000529422.1:n.116+572G>A
ENST00000529739.1:c.371G>A	ENSP00000436155.1:p.Ser124Asn
ENST00000530220.1:n.331+476G>A
ENST00000530560.5:c.338-1482G>A	ENSP00000465291.1:n.338-1482G>A
ENST00000592137.1:n.456G>A
NM_003331.4:c.3302G>A , LRG_121t1:c.3302G>A	NP_003322.3:p.Ser1101Asn
XM_011528245.1:c.3302G>A	XP_011526547.1:p.Ser1101Asn
XM_011528246.1:c.3005G>A	XP_011526548.1:p.Ser1002Asn
XM_011528247.1:c.3005G>A	XP_011526549.1:p.Ser1002Asn
XM_011528248.1:c.3200+476G>A	XP_011526550.1:n.3200+476G>A
XM_011528249.1:c.1976G>A	XP_011526551.1:p.Ser659Asn
XM_011528251.1:c.1559G>A	XP_011526553.1:p.Ser520Asn
XM_011528246.3:c.3005G>A	XP_011526548.1:p.Ser1002Asn
XM_011528249.2:c.1976G>A	XP_011526551.1:p.Ser659Asn
XR_001753750.1:n.3357+476G>A
XR_001753751.1:n.3854G>A
XR_002958353.1:n.4780G>A
NM_003331.5:c.3302G>A MANE Select	NP_003322.3:p.Ser1101Asn
NM_001385197.1:c.3302G>A	NP_001372126.1:p.Ser1101Asn
NM_001385198.1:c.3168+508G>A	NP_001372127.1:n.3168+508G>A
NM_001385199.1:c.3116G>A	NP_001372128.1:p.Ser1039Asn
NM_001385200.1:c.3299G>A	NP_001372129.1:p.Ser1100Asn
NM_001385201.1:c.3104G>A	NP_001372130.1:p.Ser1035Asn
NM_001385202.1:c.3218G>A	NP_001372131.1:p.Ser1073Asn
NM_001385203.1:c.3383G>A	NP_001372132.1:p.Ser1128Asn
NM_001385204.1:c.3512G>A	NP_001372133.1:p.Ser1171Asn
NM_001385205.1:c.3212G>A	NP_001372134.1:p.Ser1071Asn
NM_001385206.1:c.3176G>A	NP_001372135.1:p.Ser1059Asn
NM_001385207.1:c.3284G>A	NP_001372136.1:p.Ser1095Asn