Canonical Allele Identifier: CA2322387811

Gene: TYK2

Linked Data

• dbSNP Id: rs2040937872
• gnomAD v4: 19-10353823-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10353824del , CM000681.2:g.10353824del	GRCh38
NC_000019.9:g.10464500del , CM000681.1:g.10464500del	GRCh37
NC_000019.8:g.10325500del	NCBI36
NG_007872.1:g.31749del , LRG_121:g.31749del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1258-178del	ENSP00000514307.1:n.*1258-178del
ENST00000525976.6:c.2909-178del	ENSP00000434831.2:n.2909-178del
ENST00000527481.3:c.2908+218del	ENSP00000466340.2:n.2908+218del
ENST00000529370.6:n.4285-178del
ENST00000529739.2:n.3540del
ENST00000530829.2:c.*2460-178del	ENSP00000436826.2:n.*2460-178del
ENST00000531836.6:c.2909-178del	ENSP00000436175.2:n.2909-178del
ENST00000533334.2:c.*951-178del	ENSP00000432320.2:n.*951-178del
ENST00000534228.2:n.4585del
ENST00000699354.1:n.1011-178del
ENST00000699355.1:c.*2231del	ENSP00000514328.1:n.*2231del
ENST00000699356.1:n.3540del
ENST00000699357.1:n.4585del
ENST00000699358.1:c.2909-178del	ENSP00000514329.1:n.2909-178del
ENST00000699359.1:c.115-178del
ENST00000699360.1:c.2909-178del	ENSP00000514331.1:n.2909-178del
ENST00000699364.1:n.17del
ENST00000699365.1:c.-34del	ENSP00000514334.1:n.-34del
ENST00000699366.1:n.101del
ENST00000699367.1:n.101del
ENST00000699368.1:c.218del	ENSP00000514335.1:n.218del
ENST00000525621.6:c.2909-178del MANE Select	ENSP00000431885.1:n.2909-178del
ENST00000264818.10:c.2909-178del	ENSP00000264818.6:n.2909-178del
ENST00000524462.5:c.2354-178del	ENSP00000433203.1:n.2354-178del
ENST00000525621.5:c.2909-178del	ENSP00000431885.1:n.2909-178del
ENST00000527481.2:c.204+218del
ENST00000529739.1:c.-201del	ENSP00000436155.1:n.-201del
ENST00000530560.5:c.337+218del	ENSP00000465291.1:n.337+218del
ENST00000592137.1:n.63-178del
NM_003331.4:c.2909-178del , LRG_121t1:c.2909-178del	NP_003322.3:n.2909-178del
XM_011528245.1:c.2909-178del	XP_011526547.1:n.2909-178del
XM_011528246.1:c.2612-178del	XP_011526548.1:n.2612-178del
XM_011528247.1:c.2612-178del	XP_011526549.1:n.2612-178del
XM_011528248.1:c.2909-178del	XP_011526550.1:n.2909-178del
XM_011528249.1:c.1583-178del	XP_011526551.1:n.1583-178del
XM_011528251.1:c.1166-178del	XP_011526553.1:n.1166-178del
XM_011528246.3:c.2612-178del	XP_011526548.1:n.2612-178del
XM_011528249.2:c.1583-178del	XP_011526551.1:n.1583-178del
XR_001753750.1:n.3066-178del
XR_001753751.1:n.3283del
XR_002958353.1:n.4209del
NM_003331.5:c.2909-178del MANE Select	NP_003322.3:n.2909-178del
NM_001385197.1:c.2909-178del	NP_001372126.1:n.2909-178del
NM_001385198.1:c.2909-178del	NP_001372127.1:n.2909-178del
NM_001385199.1:c.2723-178del	NP_001372128.1:n.2723-178del
NM_001385200.1:c.2906-178del	NP_001372129.1:n.2906-178del
NM_001385201.1:c.2711-178del	NP_001372130.1:n.2711-178del
NM_001385202.1:c.2825-178del	NP_001372131.1:n.2825-178del
NM_001385203.1:c.2990-178del	NP_001372132.1:n.2990-178del
NM_001385204.1:c.3119-178del	NP_001372133.1:n.3119-178del
NM_001385205.1:c.2819-178del	NP_001372134.1:n.2819-178del
NM_001385206.1:c.2783-178del	NP_001372135.1:n.2783-178del
NM_001385207.1:c.2891-178del	NP_001372136.1:n.2891-178del