Canonical Allele Identifier: CA403987744

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464745T>A (hg19) ; chr19:g.10354069T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354069T>A , CM000681.2:g.10354069T>A	GRCh38
NC_000019.9:g.10464745T>A , CM000681.1:g.10464745T>A	GRCh37
NC_000019.8:g.10325745T>A	NCBI36
NG_007872.1:g.31504A>T , LRG_121:g.31504A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1230A>T	ENSP00000514307.1:n.*1230A>T
ENST00000525976.6:c.2881A>T	ENSP00000434831.2:p.Lys961Ter
ENST00000527481.3:c.2881A>T	ENSP00000466340.2:p.Lys961Ter
ENST00000529370.6:n.4257A>T
ENST00000529739.2:n.3295A>T
ENST00000530829.2:c.*2432A>T	ENSP00000436826.2:n.*2432A>T
ENST00000531836.6:c.2881A>T	ENSP00000436175.2:p.Lys961Ter
ENST00000533334.2:c.*923A>T	ENSP00000432320.2:n.*923A>T
ENST00000534228.2:n.4340A>T
ENST00000699354.1:n.983A>T
ENST00000699355.1:c.*1986A>T	ENSP00000514328.1:n.*1986A>T
ENST00000699356.1:n.3295A>T
ENST00000699357.1:n.4340A>T
ENST00000699358.1:c.2881A>T	ENSP00000514329.1:p.Lys961Ter
ENST00000699359.1:c.87A>T
ENST00000699360.1:c.2881A>T	ENSP00000514331.1:p.Lys961Ter
ENST00000699368.1:c.85A>T	ENSP00000514335.1:p.Lys29Ter
ENST00000525621.6:c.2881A>T MANE Select	ENSP00000431885.1:p.Lys961Ter
ENST00000264818.10:c.2881A>T	ENSP00000264818.6:p.Lys961Ter
ENST00000524462.5:c.2326A>T	ENSP00000433203.1:p.Lys776Ter
ENST00000525621.5:c.2881A>T	ENSP00000431885.1:p.Lys961Ter
ENST00000527481.2:c.177A>T
ENST00000529412.1:n.553A>T
ENST00000529739.1:c.-446A>T	ENSP00000436155.1:n.-446A>T
ENST00000530560.5:c.310A>T	ENSP00000465291.1:p.Lys104Ter
ENST00000592137.1:n.35A>T
NM_003331.4:c.2881A>T , LRG_121t1:c.2881A>T	NP_003322.3:p.Lys961Ter
XM_011528245.1:c.2881A>T	XP_011526547.1:p.Lys961Ter
XM_011528246.1:c.2584A>T	XP_011526548.1:p.Lys862Ter
XM_011528247.1:c.2584A>T	XP_011526549.1:p.Lys862Ter
XM_011528248.1:c.2881A>T	XP_011526550.1:p.Lys961Ter
XM_011528249.1:c.1555A>T	XP_011526551.1:p.Lys519Ter
XM_011528251.1:c.1138A>T	XP_011526553.1:p.Lys380Ter
XM_011528246.3:c.2584A>T	XP_011526548.1:p.Lys862Ter
XM_011528249.2:c.1555A>T	XP_011526551.1:p.Lys519Ter
XR_001753750.1:n.3038A>T
XR_001753751.1:n.3038A>T
XR_002958353.1:n.3964A>T
NM_003331.5:c.2881A>T MANE Select	NP_003322.3:p.Lys961Ter
NM_001385197.1:c.2881A>T	NP_001372126.1:p.Lys961Ter
NM_001385198.1:c.2881A>T	NP_001372127.1:p.Lys961Ter
NM_001385199.1:c.2695A>T	NP_001372128.1:p.Lys899Ter
NM_001385200.1:c.2878A>T	NP_001372129.1:p.Lys960Ter
NM_001385201.1:c.2683A>T	NP_001372130.1:p.Lys895Ter
NM_001385202.1:c.2797A>T	NP_001372131.1:p.Lys933Ter
NM_001385203.1:c.2962A>T	NP_001372132.1:p.Lys988Ter
NM_001385204.1:c.3091A>T	NP_001372133.1:p.Lys1031Ter
NM_001385205.1:c.2791A>T	NP_001372134.1:p.Lys931Ter
NM_001385206.1:c.2755A>T	NP_001372135.1:p.Lys919Ter
NM_001385207.1:c.2863A>T	NP_001372136.1:p.Lys955Ter