Canonical Allele Identifier: CA658799144

Gene: TYK2

Linked Data

• ClinVar Variation Id: 536655
• ClinVar RCV Id: RCV000645247 ; RCV002275095
• dbSNP Id: rs1555719851

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10365750_10365751delinsAA , CM000681.2:g.10365750_10365751delinsAA	GRCh38
NC_000019.9:g.10476426_10476427delinsAA , CM000681.1:g.10476426_10476427delinsAA	GRCh37
NC_000019.8:g.10337426_10337427delinsAA	NCBI36
NG_007872.1:g.19822_19823delinsTT , LRG_121:g.19822_19823delinsTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.777_778delinsTT	ENSP00000514307.1:p.Tyr259=
ENST00000525976.6:c.777_778delinsTT	ENSP00000434831.2:p.Tyr259=
ENST00000527481.3:c.777_778delinsTT	ENSP00000466340.2:p.Tyr259=
ENST00000529370.6:n.1108_1109delinsTT
ENST00000529739.2:n.1191_1192delinsTT
ENST00000530829.2:c.*328_*329delinsTT	ENSP00000436826.2:n.*328_*329delinsTT
ENST00000531836.6:c.777_778delinsTT	ENSP00000436175.2:p.Tyr259=
ENST00000533334.2:c.777_778delinsTT	ENSP00000432320.2:p.Tyr259=
ENST00000534228.2:n.1191_1192delinsTT
ENST00000699355.1:c.777_778delinsTT	ENSP00000514328.1:p.Tyr259=
ENST00000699356.1:n.1191_1192delinsTT
ENST00000699357.1:n.1191_1192delinsTT
ENST00000699358.1:c.777_778delinsTT	ENSP00000514329.1:p.Tyr259=
ENST00000699360.1:c.777_778delinsTT	ENSP00000514331.1:p.Tyr259=
ENST00000699369.1:n.1120_1121delinsTT
ENST00000699370.1:n.1142_1143delinsTT
ENST00000525621.6:c.777_778delinsTT MANE Select	ENSP00000431885.1:p.Tyr259=
ENST00000264818.10:c.777_778delinsTT	ENSP00000264818.6:p.Tyr259=
ENST00000524462.5:c.222_223delinsTT	ENSP00000433203.1:p.Tyr74=
ENST00000525220.1:c.113_114delinsTT
ENST00000525621.5:c.777_778delinsTT	ENSP00000431885.1:p.Tyr259=
ENST00000529370.5:c.777_778delinsTT	ENSP00000432728.1:p.Tyr259=
NM_003331.4:c.777_778delinsTT , LRG_121t1:c.777_778delinsTT	NP_003322.3:p.Tyr259=
XM_011528245.1:c.777_778delinsTT	XP_011526547.1:p.Tyr259=
XM_011528246.1:c.480_481delinsTT	XP_011526548.1:p.Tyr160=
XM_011528247.1:c.480_481delinsTT	XP_011526549.1:p.Tyr160=
XM_011528248.1:c.777_778delinsTT	XP_011526550.1:p.Tyr259=
XM_011528250.1:c.777_778delinsTT	XP_011526552.1:p.Tyr259=
XM_011528252.1:c.777_778delinsTT	XP_011526554.1:p.Tyr259=
XM_011528246.3:c.480_481delinsTT	XP_011526548.1:p.Tyr160=
XR_001753750.1:n.934_935delinsTT
XR_001753751.1:n.934_935delinsTT
XR_001753752.1:n.934_935delinsTT
XR_002958353.1:n.934_935delinsTT
NM_003331.5:c.777_778delinsTT MANE Select	NP_003322.3:p.Tyr259=
NM_001385197.1:c.777_778delinsTT	NP_001372126.1:p.Tyr259=
NM_001385198.1:c.777_778delinsTT	NP_001372127.1:p.Tyr259=
NM_001385199.1:c.777_778delinsTT	NP_001372128.1:p.Tyr259=
NM_001385200.1:c.777_778delinsTT	NP_001372129.1:p.Tyr259=
NM_001385201.1:c.777_778delinsTT	NP_001372130.1:p.Tyr259=
NM_001385202.1:c.777_778delinsTT	NP_001372131.1:p.Tyr259=
NM_001385203.1:c.777_778delinsTT	NP_001372132.1:p.Tyr259=
NM_001385204.1:c.777_778delinsTT	NP_001372133.1:p.Tyr259=
NM_001385205.1:c.687_688delinsTT	NP_001372134.1:p.Tyr229=
NM_001385206.1:c.777_778delinsTT	NP_001372135.1:p.Tyr259=
NM_001385207.1:c.777_778delinsTT	NP_001372136.1:p.Tyr259=