Canonical Allele Identifier: CA2581931584

Gene: TYK2

Linked Data

• dbSNP Id: rs749724877
• gnomAD v3: 19-10354003-GC-G
• gnomAD v4: 19-10354003-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354008del , CM000681.2:g.10354008del	GRCh38
NC_000019.9:g.10464684del , CM000681.1:g.10464684del	GRCh37
NC_000019.8:g.10325684del	NCBI36
NG_007872.1:g.31569del , LRG_121:g.31569del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1257+38del	ENSP00000514307.1:n.*1257+38del
ENST00000525976.6:c.2908+38del	ENSP00000434831.2:n.2908+38del
ENST00000527481.3:c.2908+38del	ENSP00000466340.2:n.2908+38del
ENST00000529370.6:n.4284+38del
ENST00000529739.2:n.3360del
ENST00000530829.2:c.*2459+38del	ENSP00000436826.2:n.*2459+38del
ENST00000531836.6:c.2908+38del	ENSP00000436175.2:n.2908+38del
ENST00000533334.2:c.*950+38del	ENSP00000432320.2:n.*950+38del
ENST00000534228.2:n.4405del
ENST00000699354.1:n.1010+38del
ENST00000699355.1:c.*2051del	ENSP00000514328.1:n.*2051del
ENST00000699356.1:n.3360del
ENST00000699357.1:n.4405del
ENST00000699358.1:c.2908+38del	ENSP00000514329.1:n.2908+38del
ENST00000699359.1:c.114+38del
ENST00000699360.1:c.2908+38del	ENSP00000514331.1:n.2908+38del
ENST00000699368.1:c.112+38del	ENSP00000514335.1:n.112+38del
ENST00000525621.6:c.2908+38del MANE Select	ENSP00000431885.1:n.2908+38del
ENST00000264818.10:c.2908+38del	ENSP00000264818.6:n.2908+38del
ENST00000524462.5:c.2353+38del	ENSP00000433203.1:n.2353+38del
ENST00000525621.5:c.2908+38del	ENSP00000431885.1:n.2908+38del
ENST00000527481.2:c.204+38del
ENST00000529412.1:n.618del
ENST00000529739.1:c.-381del	ENSP00000436155.1:n.-381del
ENST00000530560.5:c.337+38del	ENSP00000465291.1:n.337+38del
ENST00000592137.1:n.62+38del
NM_003331.4:c.2908+38del , LRG_121t1:c.2908+38del	NP_003322.3:n.2908+38del
XM_011528245.1:c.2908+38del	XP_011526547.1:n.2908+38del
XM_011528246.1:c.2611+38del	XP_011526548.1:n.2611+38del
XM_011528247.1:c.2611+38del	XP_011526549.1:n.2611+38del
XM_011528248.1:c.2908+38del	XP_011526550.1:n.2908+38del
XM_011528249.1:c.1582+38del	XP_011526551.1:n.1582+38del
XM_011528251.1:c.1165+38del	XP_011526553.1:n.1165+38del
XM_011528246.3:c.2611+38del	XP_011526548.1:n.2611+38del
XM_011528249.2:c.1582+38del	XP_011526551.1:n.1582+38del
XR_001753750.1:n.3065+38del
XR_001753751.1:n.3103del
XR_002958353.1:n.4029del
NM_003331.5:c.2908+38del MANE Select	NP_003322.3:n.2908+38del
NM_001385197.1:c.2908+38del	NP_001372126.1:n.2908+38del
NM_001385198.1:c.2908+38del	NP_001372127.1:n.2908+38del
NM_001385199.1:c.2722+38del	NP_001372128.1:n.2722+38del
NM_001385200.1:c.2905+38del	NP_001372129.1:n.2905+38del
NM_001385201.1:c.2710+38del	NP_001372130.1:n.2710+38del
NM_001385202.1:c.2824+38del	NP_001372131.1:n.2824+38del
NM_001385203.1:c.2989+38del	NP_001372132.1:n.2989+38del
NM_001385204.1:c.3118+38del	NP_001372133.1:n.3118+38del
NM_001385205.1:c.2818+38del	NP_001372134.1:n.2818+38del
NM_001385206.1:c.2782+38del	NP_001372135.1:n.2782+38del
NM_001385207.1:c.2890+38del	NP_001372136.1:n.2890+38del