Canonical Allele Identifier: CA305195594

Gene: TYK2

Linked Data

• dbSNP Id: rs201621864
• gnomAD v2: 19-10465717-AAAAG-A
• gnomAD v3: 19-10355041-AAAAG-A
• gnomAD v4: 19-10355041-AAAAG-A
• MyVariant Identifiers: chr19:g.10465718_10465721del (hg19) ; chr19:g.10355042_10355045del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10355057_10355060del , CM000681.2:g.10355057_10355060del	GRCh38
NC_000019.9:g.10465733_10465736del , CM000681.1:g.10465733_10465736del	GRCh37
NC_000019.8:g.10326733_10326736del	NCBI36
NG_007872.1:g.30528_30531del , LRG_121:g.30528_30531del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*967-436_*967-433del	ENSP00000514307.1:n.*967-436_*967-433del
ENST00000525976.6:c.2618-436_2618-433del	ENSP00000434831.2:n.2618-436_2618-433del
ENST00000527481.3:c.2618-436_2618-433del	ENSP00000466340.2:n.2618-436_2618-433del
ENST00000529370.6:n.3994-436_3994-433del
ENST00000529739.2:n.3032-436_3032-433del
ENST00000530829.2:c.*2169-436_*2169-433del	ENSP00000436826.2:n.*2169-436_*2169-433del
ENST00000531836.6:c.2618-436_2618-433del	ENSP00000436175.2:n.2618-436_2618-433del
ENST00000533334.2:c.*660-436_*660-433del	ENSP00000432320.2:n.*660-436_*660-433del
ENST00000534228.2:n.4077-436_4077-433del
ENST00000699354.1:n.720-436_720-433del
ENST00000699355.1:c.*1723-436_*1723-433del	ENSP00000514328.1:n.*1723-436_*1723-433del
ENST00000699356.1:n.3032-436_3032-433del
ENST00000699357.1:n.4077-436_4077-433del
ENST00000699358.1:c.2618-436_2618-433del	ENSP00000514329.1:n.2618-436_2618-433del
ENST00000699360.1:c.2618-436_2618-433del	ENSP00000514331.1:n.2618-436_2618-433del
ENST00000525621.6:c.2618-436_2618-433del MANE Select	ENSP00000431885.1:n.2618-436_2618-433del
ENST00000264818.10:c.2618-436_2618-433del	ENSP00000264818.6:n.2618-436_2618-433del
ENST00000524462.5:c.2063-436_2063-433del	ENSP00000433203.1:n.2063-436_2063-433del
ENST00000525621.5:c.2618-436_2618-433del	ENSP00000431885.1:n.2618-436_2618-433del
ENST00000529412.1:n.290-436_290-433del
ENST00000530560.5:c.47-436_47-433del	ENSP00000465291.1:n.47-436_47-433del
ENST00000534228.1:n.518-436_518-433del
NM_003331.4:c.2618-436_2618-433del , LRG_121t1:c.2618-436_2618-433del	NP_003322.3:n.2618-436_2618-433del
XM_011528245.1:c.2618-436_2618-433del	XP_011526547.1:n.2618-436_2618-433del
XM_011528246.1:c.2321-436_2321-433del	XP_011526548.1:n.2321-436_2321-433del
XM_011528247.1:c.2321-436_2321-433del	XP_011526549.1:n.2321-436_2321-433del
XM_011528248.1:c.2618-436_2618-433del	XP_011526550.1:n.2618-436_2618-433del
XM_011528249.1:c.1292-436_1292-433del	XP_011526551.1:n.1292-436_1292-433del
XM_011528251.1:c.875-436_875-433del	XP_011526553.1:n.875-436_875-433del
XM_011528246.3:c.2321-436_2321-433del	XP_011526548.1:n.2321-436_2321-433del
XM_011528249.2:c.1292-436_1292-433del	XP_011526551.1:n.1292-436_1292-433del
XR_001753750.1:n.2775-436_2775-433del
XR_001753751.1:n.2775-436_2775-433del
XR_002958353.1:n.3701-436_3701-433del
NM_003331.5:c.2618-436_2618-433del MANE Select	NP_003322.3:n.2618-436_2618-433del
NM_001385197.1:c.2618-436_2618-433del	NP_001372126.1:n.2618-436_2618-433del
NM_001385198.1:c.2618-436_2618-433del	NP_001372127.1:n.2618-436_2618-433del
NM_001385199.1:c.2432-436_2432-433del	NP_001372128.1:n.2432-436_2432-433del
NM_001385200.1:c.2615-436_2615-433del	NP_001372129.1:n.2615-436_2615-433del
NM_001385201.1:c.2420-436_2420-433del	NP_001372130.1:n.2420-436_2420-433del
NM_001385202.1:c.2534-436_2534-433del	NP_001372131.1:n.2534-436_2534-433del
NM_001385203.1:c.2618-163_2618-160del	NP_001372132.1:n.2618-163_2618-160del
NM_001385204.1:c.2828-436_2828-433del	NP_001372133.1:n.2828-436_2828-433del
NM_001385205.1:c.2528-436_2528-433del	NP_001372134.1:n.2528-436_2528-433del
NM_001385206.1:c.2492-436_2492-433del	NP_001372135.1:n.2492-436_2492-433del
NM_001385207.1:c.2600-436_2600-433del	NP_001372136.1:n.2600-436_2600-433del