Canonical Allele Identifier: CA631725139

Gene: TYK2

Linked Data

• dbSNP Id: rs1474432133
• gnomAD v2: 19-10465444-AATG-A
• gnomAD v3: 19-10354768-AATG-A
• gnomAD v4: 19-10354768-AATG-A
• MyVariant Identifiers: chr19:g.10465445_10465447del (hg19) ; chr19:g.10354769_10354771del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354772_10354774del , CM000681.2:g.10354772_10354774del	GRCh38
NC_000019.9:g.10465448_10465450del , CM000681.1:g.10465448_10465450del	GRCh37
NC_000019.8:g.10326448_10326450del	NCBI36
NG_007872.1:g.30802_30804del , LRG_121:g.30802_30804del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*967-162_*967-160del	ENSP00000514307.1:n.*967-162_*967-160del
ENST00000525976.6:c.2618-162_2618-160del	ENSP00000434831.2:n.2618-162_2618-160del
ENST00000527481.3:c.2618-162_2618-160del	ENSP00000466340.2:n.2618-162_2618-160del
ENST00000529370.6:n.3994-162_3994-160del
ENST00000529739.2:n.3032-162_3032-160del
ENST00000530829.2:c.*2169-162_*2169-160del	ENSP00000436826.2:n.*2169-162_*2169-160del
ENST00000531836.6:c.2618-162_2618-160del	ENSP00000436175.2:n.2618-162_2618-160del
ENST00000533334.2:c.*660-162_*660-160del	ENSP00000432320.2:n.*660-162_*660-160del
ENST00000534228.2:n.4077-162_4077-160del
ENST00000699354.1:n.720-162_720-160del
ENST00000699355.1:c.*1723-162_*1723-160del	ENSP00000514328.1:n.*1723-162_*1723-160del
ENST00000699356.1:n.3032-162_3032-160del
ENST00000699357.1:n.4077-162_4077-160del
ENST00000699358.1:c.2618-162_2618-160del	ENSP00000514329.1:n.2618-162_2618-160del
ENST00000699360.1:c.2618-162_2618-160del	ENSP00000514331.1:n.2618-162_2618-160del
ENST00000525621.6:c.2618-162_2618-160del MANE Select	ENSP00000431885.1:n.2618-162_2618-160del
ENST00000264818.10:c.2618-162_2618-160del	ENSP00000264818.6:n.2618-162_2618-160del
ENST00000524462.5:c.2063-162_2063-160del	ENSP00000433203.1:n.2063-162_2063-160del
ENST00000525621.5:c.2618-162_2618-160del	ENSP00000431885.1:n.2618-162_2618-160del
ENST00000529412.1:n.290-162_290-160del
ENST00000530560.5:c.47-162_47-160del	ENSP00000465291.1:n.47-162_47-160del
ENST00000534228.1:n.518-162_518-160del
NM_003331.4:c.2618-162_2618-160del , LRG_121t1:c.2618-162_2618-160del	NP_003322.3:n.2618-162_2618-160del
XM_011528245.1:c.2618-162_2618-160del	XP_011526547.1:n.2618-162_2618-160del
XM_011528246.1:c.2321-162_2321-160del	XP_011526548.1:n.2321-162_2321-160del
XM_011528247.1:c.2321-162_2321-160del	XP_011526549.1:n.2321-162_2321-160del
XM_011528248.1:c.2618-162_2618-160del	XP_011526550.1:n.2618-162_2618-160del
XM_011528249.1:c.1292-162_1292-160del	XP_011526551.1:n.1292-162_1292-160del
XM_011528251.1:c.875-162_875-160del	XP_011526553.1:n.875-162_875-160del
XM_011528246.3:c.2321-162_2321-160del	XP_011526548.1:n.2321-162_2321-160del
XM_011528249.2:c.1292-162_1292-160del	XP_011526551.1:n.1292-162_1292-160del
XR_001753750.1:n.2775-162_2775-160del
XR_001753751.1:n.2775-162_2775-160del
XR_002958353.1:n.3701-162_3701-160del
NM_003331.5:c.2618-162_2618-160del MANE Select	NP_003322.3:n.2618-162_2618-160del
NM_001385197.1:c.2618-162_2618-160del	NP_001372126.1:n.2618-162_2618-160del
NM_001385198.1:c.2618-162_2618-160del	NP_001372127.1:n.2618-162_2618-160del
NM_001385199.1:c.2432-162_2432-160del	NP_001372128.1:n.2432-162_2432-160del
NM_001385200.1:c.2615-162_2615-160del	NP_001372129.1:n.2615-162_2615-160del
NM_001385201.1:c.2420-162_2420-160del	NP_001372130.1:n.2420-162_2420-160del
NM_001385202.1:c.2534-162_2534-160del	NP_001372131.1:n.2534-162_2534-160del
NM_001385203.1:c.2698+31_2698+33del	NP_001372132.1:n.2698+31_2698+33del
NM_001385204.1:c.2828-162_2828-160del	NP_001372133.1:n.2828-162_2828-160del
NM_001385205.1:c.2528-162_2528-160del	NP_001372134.1:n.2528-162_2528-160del
NM_001385206.1:c.2492-162_2492-160del	NP_001372135.1:n.2492-162_2492-160del
NM_001385207.1:c.2600-162_2600-160del	NP_001372136.1:n.2600-162_2600-160del