Canonical Allele Identifier: CA2322387443

Gene: TYK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352682C= , CM000681.2:g.10352682C=	GRCh38
NC_000019.9:g.10463358C= , CM000681.1:g.10463358C=	GRCh37
NC_000019.8:g.10324358C=	NCBI36
NG_007872.1:g.32891G= , LRG_121:g.32891G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1550-131G=	ENSP00000514307.1:n.*1550-131G=
ENST00000525976.6:c.3201-131G=	ENSP00000434831.2:n.3201-131G=
ENST00000527481.3:c.3082-131G=	ENSP00000466340.2:n.3082-131G=
ENST00000529370.6:n.4577-131G=
ENST00000529739.2:n.4010-131G=
ENST00000530829.2:c.*2752-131G=	ENSP00000436826.2:n.*2752-131G=
ENST00000531836.6:c.3201-131G=	ENSP00000436175.2:n.3201-131G=
ENST00000533334.2:c.*1242+244G=	ENSP00000432320.2:n.*1242+244G=
ENST00000534228.2:n.5054+244G=
ENST00000699354.1:n.1303-131G=
ENST00000699355.1:c.*2701-131G=	ENSP00000514328.1:n.*2701-131G=
ENST00000699356.1:n.4010-131G=
ENST00000699357.1:n.5055-131G=
ENST00000699358.1:c.3200+244G=	ENSP00000514329.1:n.3200+244G=
ENST00000699359.1:c.375-131G=
ENST00000699360.1:c.3159-131G=	ENSP00000514331.1:n.3159-131G=
ENST00000699361.1:n.104G=
ENST00000699362.1:c.97-131G=	ENSP00000514332.1:n.97-131G=
ENST00000699363.1:c.97-131G=	ENSP00000514333.1:n.97-131G=
ENST00000699364.1:n.201-131G=
ENST00000699365.1:c.270-131G=	ENSP00000514334.1:n.270-131G=
ENST00000699366.1:n.111+1132G=
ENST00000699367.1:n.111+1132G=
ENST00000699368.1:c.688-131G=	ENSP00000514335.1:n.688-131G=
ENST00000525621.6:c.3201-131G= MANE Select	ENSP00000431885.1:n.3201-131G=
ENST00000264818.10:c.3201-131G=	ENSP00000264818.6:n.3201-131G=
ENST00000524462.5:c.2646-131G=	ENSP00000433203.1:n.2646-131G=
ENST00000525621.5:c.3201-131G=	ENSP00000431885.1:n.3201-131G=
ENST00000527481.2:c.378-131G=
ENST00000529422.1:n.116+340G=
ENST00000529739.1:c.270-131G=	ENSP00000436155.1:n.270-131G=
ENST00000530220.1:n.331+244G=
ENST00000530560.5:c.337+1360G=	ENSP00000465291.1:n.337+1360G=
ENST00000592137.1:n.355-131G=
NM_003331.4:c.3201-131G= , LRG_121t1:c.3201-131G=	NP_003322.3:n.3201-131G=
XM_011528245.1:c.3201-131G=	XP_011526547.1:n.3201-131G=
XM_011528246.1:c.2904-131G=	XP_011526548.1:n.2904-131G=
XM_011528247.1:c.2904-131G=	XP_011526549.1:n.2904-131G=
XM_011528248.1:c.3200+244G=	XP_011526550.1:n.3200+244G=
XM_011528249.1:c.1875-131G=	XP_011526551.1:n.1875-131G=
XM_011528251.1:c.1458-131G=	XP_011526553.1:n.1458-131G=
XM_011528246.3:c.2904-131G=	XP_011526548.1:n.2904-131G=
XM_011528249.2:c.1875-131G=	XP_011526551.1:n.1875-131G=
XR_001753750.1:n.3357+244G=
XR_001753751.1:n.3753-131G=
XR_002958353.1:n.4679-131G=
NM_003331.5:c.3201-131G= MANE Select	NP_003322.3:n.3201-131G=
NM_001385197.1:c.3201-131G=	NP_001372126.1:n.3201-131G=
NM_001385198.1:c.3168+276G=	NP_001372127.1:n.3168+276G=
NM_001385199.1:c.3015-131G=	NP_001372128.1:n.3015-131G=
NM_001385200.1:c.3198-131G=	NP_001372129.1:n.3198-131G=
NM_001385201.1:c.3003-131G=	NP_001372130.1:n.3003-131G=
NM_001385202.1:c.3117-131G=	NP_001372131.1:n.3117-131G=
NM_001385203.1:c.3282-131G=	NP_001372132.1:n.3282-131G=
NM_001385204.1:c.3411-131G=	NP_001372133.1:n.3411-131G=
NM_001385205.1:c.3111-131G=	NP_001372134.1:n.3111-131G=
NM_001385206.1:c.3075-131G=	NP_001372135.1:n.3075-131G=
NM_001385207.1:c.3183-131G=	NP_001372136.1:n.3183-131G=