Canonical Allele Identifier: CA657204828

Gene: TYK2

Linked Data

• COSMIC: COSN23559556

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10355052_10355053insAGTA , CM000681.2:g.10355052_10355053insAGTA	GRCh38
NC_000019.9:g.10465728_10465729insAGTA , CM000681.1:g.10465728_10465729insAGTA	GRCh37
NC_000019.8:g.10326728_10326729insAGTA	NCBI36
NG_007872.1:g.30521_30522insACTT , LRG_121:g.30521_30522insACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*967-443_*967-442insACTT	ENSP00000514307.1:n.*967-443_*967-442insACTT
ENST00000525976.6:c.2618-443_2618-442insACTT	ENSP00000434831.2:n.2618-443_2618-442insACTT
ENST00000527481.3:c.2618-443_2618-442insACTT	ENSP00000466340.2:n.2618-443_2618-442insACTT
ENST00000529370.6:n.3994-443_3994-442insACTT
ENST00000529739.2:n.3032-443_3032-442insACTT
ENST00000530829.2:c.*2169-443_*2169-442insACTT	ENSP00000436826.2:n.*2169-443_*2169-442insACTT
ENST00000531836.6:c.2618-443_2618-442insACTT	ENSP00000436175.2:n.2618-443_2618-442insACTT
ENST00000533334.2:c.*660-443_*660-442insACTT	ENSP00000432320.2:n.*660-443_*660-442insACTT
ENST00000534228.2:n.4077-443_4077-442insACTT
ENST00000699354.1:n.720-443_720-442insACTT
ENST00000699355.1:c.*1723-443_*1723-442insACTT	ENSP00000514328.1:n.*1723-443_*1723-442insACTT
ENST00000699356.1:n.3032-443_3032-442insACTT
ENST00000699357.1:n.4077-443_4077-442insACTT
ENST00000699358.1:c.2618-443_2618-442insACTT	ENSP00000514329.1:n.2618-443_2618-442insACTT
ENST00000699360.1:c.2618-443_2618-442insACTT	ENSP00000514331.1:n.2618-443_2618-442insACTT
ENST00000525621.6:c.2618-443_2618-442insACTT MANE Select	ENSP00000431885.1:n.2618-443_2618-442insACTT
ENST00000264818.10:c.2618-443_2618-442insACTT	ENSP00000264818.6:n.2618-443_2618-442insACTT
ENST00000524462.5:c.2063-443_2063-442insACTT	ENSP00000433203.1:n.2063-443_2063-442insACTT
ENST00000525621.5:c.2618-443_2618-442insACTT	ENSP00000431885.1:n.2618-443_2618-442insACTT
ENST00000529412.1:n.290-443_290-442insACTT
ENST00000530560.5:c.47-443_47-442insACTT	ENSP00000465291.1:n.47-443_47-442insACTT
ENST00000534228.1:n.518-443_518-442insACTT
NM_003331.4:c.2618-443_2618-442insACTT , LRG_121t1:c.2618-443_2618-442insACTT	NP_003322.3:n.2618-443_2618-442insACTT
XM_011528245.1:c.2618-443_2618-442insACTT	XP_011526547.1:n.2618-443_2618-442insACTT
XM_011528246.1:c.2321-443_2321-442insACTT	XP_011526548.1:n.2321-443_2321-442insACTT
XM_011528247.1:c.2321-443_2321-442insACTT	XP_011526549.1:n.2321-443_2321-442insACTT
XM_011528248.1:c.2618-443_2618-442insACTT	XP_011526550.1:n.2618-443_2618-442insACTT
XM_011528249.1:c.1292-443_1292-442insACTT	XP_011526551.1:n.1292-443_1292-442insACTT
XM_011528251.1:c.875-443_875-442insACTT	XP_011526553.1:n.875-443_875-442insACTT
XM_011528246.3:c.2321-443_2321-442insACTT	XP_011526548.1:n.2321-443_2321-442insACTT
XM_011528249.2:c.1292-443_1292-442insACTT	XP_011526551.1:n.1292-443_1292-442insACTT
XR_001753750.1:n.2775-443_2775-442insACTT
XR_001753751.1:n.2775-443_2775-442insACTT
XR_002958353.1:n.3701-443_3701-442insACTT
NM_003331.5:c.2618-443_2618-442insACTT MANE Select	NP_003322.3:n.2618-443_2618-442insACTT
NM_001385197.1:c.2618-443_2618-442insACTT	NP_001372126.1:n.2618-443_2618-442insACTT
NM_001385198.1:c.2618-443_2618-442insACTT	NP_001372127.1:n.2618-443_2618-442insACTT
NM_001385199.1:c.2432-443_2432-442insACTT	NP_001372128.1:n.2432-443_2432-442insACTT
NM_001385200.1:c.2615-443_2615-442insACTT	NP_001372129.1:n.2615-443_2615-442insACTT
NM_001385201.1:c.2420-443_2420-442insACTT	NP_001372130.1:n.2420-443_2420-442insACTT
NM_001385202.1:c.2534-443_2534-442insACTT	NP_001372131.1:n.2534-443_2534-442insACTT
NM_001385203.1:c.2618-170_2618-169insACTT	NP_001372132.1:n.2618-170_2618-169insACTT
NM_001385204.1:c.2828-443_2828-442insACTT	NP_001372133.1:n.2828-443_2828-442insACTT
NM_001385205.1:c.2528-443_2528-442insACTT	NP_001372134.1:n.2528-443_2528-442insACTT
NM_001385206.1:c.2492-443_2492-442insACTT	NP_001372135.1:n.2492-443_2492-442insACTT
NM_001385207.1:c.2600-443_2600-442insACTT	NP_001372136.1:n.2600-443_2600-442insACTT