Canonical Allele Identifier: CA2322393366

Gene: TYK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10365442_10365444delinsTAG , CM000681.2:g.10365442_10365444delinsTAG	GRCh38
NC_000019.9:g.10476118_10476120delinsTAG , CM000681.1:g.10476118_10476120delinsTAG	GRCh37
NC_000019.8:g.10337118_10337120delinsTAG	NCBI36
NG_007872.1:g.20129_20131delinsCTA , LRG_121:g.20129_20131delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.1011+73_1011+75delinsCTA	ENSP00000514307.1:n.1011+73_1011+75delinsCTA
ENST00000525976.6:c.1011+73_1011+75delinsCTA	ENSP00000434831.2:n.1011+73_1011+75delinsCTA
ENST00000527481.3:c.1011+73_1011+75delinsCTA	ENSP00000466340.2:n.1011+73_1011+75delinsCTA
ENST00000529370.6:n.1342+73_1342+75delinsCTA
ENST00000529739.2:n.1425+73_1425+75delinsCTA
ENST00000530829.2:c.*562+73_*562+75delinsCTA	ENSP00000436826.2:n.*562+73_*562+75delinsCTA
ENST00000531836.6:c.1011+73_1011+75delinsCTA	ENSP00000436175.2:n.1011+73_1011+75delinsCTA
ENST00000533334.2:c.1011+73_1011+75delinsCTA	ENSP00000432320.2:n.1011+73_1011+75delinsCTA
ENST00000534228.2:n.1425+73_1425+75delinsCTA
ENST00000699355.1:c.1011+73_1011+75delinsCTA	ENSP00000514328.1:n.1011+73_1011+75delinsCTA
ENST00000699356.1:n.1425+73_1425+75delinsCTA
ENST00000699357.1:n.1425+73_1425+75delinsCTA
ENST00000699358.1:c.1011+73_1011+75delinsCTA	ENSP00000514329.1:n.1011+73_1011+75delinsCTA
ENST00000699360.1:c.1011+73_1011+75delinsCTA	ENSP00000514331.1:n.1011+73_1011+75delinsCTA
ENST00000699369.1:n.1427_1429delinsCTA
ENST00000699370.1:n.1449_1451delinsCTA
ENST00000525621.6:c.1011+73_1011+75delinsCTA MANE Select	ENSP00000431885.1:n.1011+73_1011+75delinsCTA
ENST00000264818.10:c.1011+73_1011+75delinsCTA	ENSP00000264818.6:n.1011+73_1011+75delinsCTA
ENST00000524462.5:c.456+73_456+75delinsCTA	ENSP00000433203.1:n.456+73_456+75delinsCTA
ENST00000525220.1:c.347+73_347+75delinsCTA
ENST00000525621.5:c.1011+73_1011+75delinsCTA	ENSP00000431885.1:n.1011+73_1011+75delinsCTA
ENST00000529370.5:c.1011+73_1011+75delinsCTA	ENSP00000432728.1:n.1011+73_1011+75delinsCTA
NM_003331.4:c.1011+73_1011+75delinsCTA , LRG_121t1:c.1011+73_1011+75delinsCTA	NP_003322.3:n.1011+73_1011+75delinsCTA
XM_011528245.1:c.1011+73_1011+75delinsCTA	XP_011526547.1:n.1011+73_1011+75delinsCTA
XM_011528246.1:c.714+73_714+75delinsCTA	XP_011526548.1:n.714+73_714+75delinsCTA
XM_011528247.1:c.714+73_714+75delinsCTA	XP_011526549.1:n.714+73_714+75delinsCTA
XM_011528248.1:c.1011+73_1011+75delinsCTA	XP_011526550.1:n.1011+73_1011+75delinsCTA
XM_011528250.1:c.1011+73_1011+75delinsCTA	XP_011526552.1:n.1011+73_1011+75delinsCTA
XM_011528252.1:c.1011+73_1011+75delinsCTA	XP_011526554.1:n.1011+73_1011+75delinsCTA
XM_011528246.3:c.714+73_714+75delinsCTA	XP_011526548.1:n.714+73_714+75delinsCTA
XR_001753750.1:n.1168+73_1168+75delinsCTA
XR_001753751.1:n.1168+73_1168+75delinsCTA
XR_001753752.1:n.1168+73_1168+75delinsCTA
XR_002958353.1:n.1168+73_1168+75delinsCTA
NM_003331.5:c.1011+73_1011+75delinsCTA MANE Select	NP_003322.3:n.1011+73_1011+75delinsCTA
NM_001385197.1:c.1011+73_1011+75delinsCTA	NP_001372126.1:n.1011+73_1011+75delinsCTA
NM_001385198.1:c.1011+73_1011+75delinsCTA	NP_001372127.1:n.1011+73_1011+75delinsCTA
NM_001385199.1:c.1011+73_1011+75delinsCTA	NP_001372128.1:n.1011+73_1011+75delinsCTA
NM_001385200.1:c.1011+73_1011+75delinsCTA	NP_001372129.1:n.1011+73_1011+75delinsCTA
NM_001385201.1:c.1011+73_1011+75delinsCTA	NP_001372130.1:n.1011+73_1011+75delinsCTA
NM_001385202.1:c.1011+73_1011+75delinsCTA	NP_001372131.1:n.1011+73_1011+75delinsCTA
NM_001385203.1:c.1011+73_1011+75delinsCTA	NP_001372132.1:n.1011+73_1011+75delinsCTA
NM_001385204.1:c.1011+73_1011+75delinsCTA	NP_001372133.1:n.1011+73_1011+75delinsCTA
NM_001385205.1:c.921+73_921+75delinsCTA	NP_001372134.1:n.921+73_921+75delinsCTA
NM_001385206.1:c.1011+73_1011+75delinsCTA	NP_001372135.1:n.1011+73_1011+75delinsCTA
NM_001385207.1:c.1011+73_1011+75delinsCTA	NP_001372136.1:n.1011+73_1011+75delinsCTA