Canonical Allele Identifier: CA783143254

Gene: TYK2

Linked Data

• dbSNP Id: rs1192317805
• MyVariant Identifiers: chr19:g.10465625_10465627del (hg19) ; chr19:g.10354949_10354951del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354952_10354954del , CM000681.2:g.10354952_10354954del	GRCh38
NC_000019.9:g.10465628_10465630del , CM000681.1:g.10465628_10465630del	GRCh37
NC_000019.8:g.10326628_10326630del	NCBI36
NG_007872.1:g.30622_30624del , LRG_121:g.30622_30624del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*967-342_*967-340del	ENSP00000514307.1:n.*967-342_*967-340del
ENST00000525976.6:c.2618-342_2618-340del	ENSP00000434831.2:n.2618-342_2618-340del
ENST00000527481.3:c.2618-342_2618-340del	ENSP00000466340.2:n.2618-342_2618-340del
ENST00000529370.6:n.3994-342_3994-340del
ENST00000529739.2:n.3032-342_3032-340del
ENST00000530829.2:c.*2169-342_*2169-340del	ENSP00000436826.2:n.*2169-342_*2169-340del
ENST00000531836.6:c.2618-342_2618-340del	ENSP00000436175.2:n.2618-342_2618-340del
ENST00000533334.2:c.*660-342_*660-340del	ENSP00000432320.2:n.*660-342_*660-340del
ENST00000534228.2:n.4077-342_4077-340del
ENST00000699354.1:n.720-342_720-340del
ENST00000699355.1:c.*1723-342_*1723-340del	ENSP00000514328.1:n.*1723-342_*1723-340del
ENST00000699356.1:n.3032-342_3032-340del
ENST00000699357.1:n.4077-342_4077-340del
ENST00000699358.1:c.2618-342_2618-340del	ENSP00000514329.1:n.2618-342_2618-340del
ENST00000699360.1:c.2618-342_2618-340del	ENSP00000514331.1:n.2618-342_2618-340del
ENST00000525621.6:c.2618-342_2618-340del MANE Select	ENSP00000431885.1:n.2618-342_2618-340del
ENST00000264818.10:c.2618-342_2618-340del	ENSP00000264818.6:n.2618-342_2618-340del
ENST00000524462.5:c.2063-342_2063-340del	ENSP00000433203.1:n.2063-342_2063-340del
ENST00000525621.5:c.2618-342_2618-340del	ENSP00000431885.1:n.2618-342_2618-340del
ENST00000529412.1:n.290-342_290-340del
ENST00000530560.5:c.47-342_47-340del	ENSP00000465291.1:n.47-342_47-340del
ENST00000534228.1:n.518-342_518-340del
NM_003331.4:c.2618-342_2618-340del , LRG_121t1:c.2618-342_2618-340del	NP_003322.3:n.2618-342_2618-340del
XM_011528245.1:c.2618-342_2618-340del	XP_011526547.1:n.2618-342_2618-340del
XM_011528246.1:c.2321-342_2321-340del	XP_011526548.1:n.2321-342_2321-340del
XM_011528247.1:c.2321-342_2321-340del	XP_011526549.1:n.2321-342_2321-340del
XM_011528248.1:c.2618-342_2618-340del	XP_011526550.1:n.2618-342_2618-340del
XM_011528249.1:c.1292-342_1292-340del	XP_011526551.1:n.1292-342_1292-340del
XM_011528251.1:c.875-342_875-340del	XP_011526553.1:n.875-342_875-340del
XM_011528246.3:c.2321-342_2321-340del	XP_011526548.1:n.2321-342_2321-340del
XM_011528249.2:c.1292-342_1292-340del	XP_011526551.1:n.1292-342_1292-340del
XR_001753750.1:n.2775-342_2775-340del
XR_001753751.1:n.2775-342_2775-340del
XR_002958353.1:n.3701-342_3701-340del
NM_003331.5:c.2618-342_2618-340del MANE Select	NP_003322.3:n.2618-342_2618-340del
NM_001385197.1:c.2618-342_2618-340del	NP_001372126.1:n.2618-342_2618-340del
NM_001385198.1:c.2618-342_2618-340del	NP_001372127.1:n.2618-342_2618-340del
NM_001385199.1:c.2432-342_2432-340del	NP_001372128.1:n.2432-342_2432-340del
NM_001385200.1:c.2615-342_2615-340del	NP_001372129.1:n.2615-342_2615-340del
NM_001385201.1:c.2420-342_2420-340del	NP_001372130.1:n.2420-342_2420-340del
NM_001385202.1:c.2534-342_2534-340del	NP_001372131.1:n.2534-342_2534-340del
NM_001385203.1:c.2618-69_2618-67del	NP_001372132.1:n.2618-69_2618-67del
NM_001385204.1:c.2828-342_2828-340del	NP_001372133.1:n.2828-342_2828-340del
NM_001385205.1:c.2528-342_2528-340del	NP_001372134.1:n.2528-342_2528-340del
NM_001385206.1:c.2492-342_2492-340del	NP_001372135.1:n.2492-342_2492-340del
NM_001385207.1:c.2600-342_2600-340del	NP_001372136.1:n.2600-342_2600-340del