Canonical Allele Identifier: CA2582371274

Gene: TYK2

Linked Data

• gnomAD v4: 19-10353833-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10353833C>A , CM000681.2:g.10353833C>A	GRCh38
NC_000019.9:g.10464509C>A , CM000681.1:g.10464509C>A	GRCh37
NC_000019.8:g.10325509C>A	NCBI36
NG_007872.1:g.31740G>T , LRG_121:g.31740G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1258-187G>T	ENSP00000514307.1:n.*1258-187G>T
ENST00000525976.6:c.2909-187G>T	ENSP00000434831.2:n.2909-187G>T
ENST00000527481.3:c.2908+209G>T	ENSP00000466340.2:n.2908+209G>T
ENST00000529370.6:n.4285-187G>T
ENST00000529739.2:n.3531G>T
ENST00000530829.2:c.*2460-187G>T	ENSP00000436826.2:n.*2460-187G>T
ENST00000531836.6:c.2909-187G>T	ENSP00000436175.2:n.2909-187G>T
ENST00000533334.2:c.*951-187G>T	ENSP00000432320.2:n.*951-187G>T
ENST00000534228.2:n.4576G>T
ENST00000699354.1:n.1011-187G>T
ENST00000699355.1:c.*2222G>T	ENSP00000514328.1:n.*2222G>T
ENST00000699356.1:n.3531G>T
ENST00000699357.1:n.4576G>T
ENST00000699358.1:c.2909-187G>T	ENSP00000514329.1:n.2909-187G>T
ENST00000699359.1:c.115-187G>T
ENST00000699360.1:c.2909-187G>T	ENSP00000514331.1:n.2909-187G>T
ENST00000699364.1:n.8G>T
ENST00000699365.1:c.-43G>T	ENSP00000514334.1:n.-43G>T
ENST00000699366.1:n.92G>T
ENST00000699367.1:n.92G>T
ENST00000699368.1:c.209G>T	ENSP00000514335.1:n.209G>T
ENST00000525621.6:c.2909-187G>T MANE Select	ENSP00000431885.1:n.2909-187G>T
ENST00000264818.10:c.2909-187G>T	ENSP00000264818.6:n.2909-187G>T
ENST00000524462.5:c.2354-187G>T	ENSP00000433203.1:n.2354-187G>T
ENST00000525621.5:c.2909-187G>T	ENSP00000431885.1:n.2909-187G>T
ENST00000527481.2:c.204+209G>T
ENST00000529739.1:c.-210G>T	ENSP00000436155.1:n.-210G>T
ENST00000530560.5:c.337+209G>T	ENSP00000465291.1:n.337+209G>T
ENST00000592137.1:n.63-187G>T
NM_003331.4:c.2909-187G>T , LRG_121t1:c.2909-187G>T	NP_003322.3:n.2909-187G>T
XM_011528245.1:c.2909-187G>T	XP_011526547.1:n.2909-187G>T
XM_011528246.1:c.2612-187G>T	XP_011526548.1:n.2612-187G>T
XM_011528247.1:c.2612-187G>T	XP_011526549.1:n.2612-187G>T
XM_011528248.1:c.2909-187G>T	XP_011526550.1:n.2909-187G>T
XM_011528249.1:c.1583-187G>T	XP_011526551.1:n.1583-187G>T
XM_011528251.1:c.1166-187G>T	XP_011526553.1:n.1166-187G>T
XM_011528246.3:c.2612-187G>T	XP_011526548.1:n.2612-187G>T
XM_011528249.2:c.1583-187G>T	XP_011526551.1:n.1583-187G>T
XR_001753750.1:n.3066-187G>T
XR_001753751.1:n.3274G>T
XR_002958353.1:n.4200G>T
NM_003331.5:c.2909-187G>T MANE Select	NP_003322.3:n.2909-187G>T
NM_001385197.1:c.2909-187G>T	NP_001372126.1:n.2909-187G>T
NM_001385198.1:c.2909-187G>T	NP_001372127.1:n.2909-187G>T
NM_001385199.1:c.2723-187G>T	NP_001372128.1:n.2723-187G>T
NM_001385200.1:c.2906-187G>T	NP_001372129.1:n.2906-187G>T
NM_001385201.1:c.2711-187G>T	NP_001372130.1:n.2711-187G>T
NM_001385202.1:c.2825-187G>T	NP_001372131.1:n.2825-187G>T
NM_001385203.1:c.2990-187G>T	NP_001372132.1:n.2990-187G>T
NM_001385204.1:c.3119-187G>T	NP_001372133.1:n.3119-187G>T
NM_001385205.1:c.2819-187G>T	NP_001372134.1:n.2819-187G>T
NM_001385206.1:c.2783-187G>T	NP_001372135.1:n.2783-187G>T
NM_001385207.1:c.2891-187G>T	NP_001372136.1:n.2891-187G>T