Canonical Allele Identifier: CA505371116

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463140C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352464C>G , CM000681.2:g.10352464C>G	GRCh38
NC_000019.9:g.10463140C>G , CM000681.1:g.10463140C>G	GRCh37
NC_000019.8:g.10324140C>G	NCBI36
NG_007872.1:g.33109G>C , LRG_121:g.33109G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1637G>C	ENSP00000514307.1:n.*1637G>C
ENST00000525976.6:c.3288G>C	ENSP00000434831.2:p.Thr1096=
ENST00000527481.3:c.*58G>C	ENSP00000466340.2:n.*58G>C
ENST00000529370.6:n.4664G>C
ENST00000529739.2:n.4097G>C
ENST00000530829.2:c.*2839G>C	ENSP00000436826.2:n.*2839G>C
ENST00000531836.6:c.3288G>C	ENSP00000436175.2:p.Thr1096=
ENST00000533334.2:c.*1242+462G>C	ENSP00000432320.2:n.*1242+462G>C
ENST00000534228.2:n.5054+462G>C
ENST00000699354.1:n.1390G>C
ENST00000699355.1:c.*2788G>C	ENSP00000514328.1:n.*2788G>C
ENST00000699356.1:n.4097G>C
ENST00000699357.1:n.5142G>C
ENST00000699358.1:c.3200+462G>C	ENSP00000514329.1:n.3200+462G>C
ENST00000699359.1:c.462G>C
ENST00000699360.1:c.3246G>C	ENSP00000514331.1:p.Thr1082=
ENST00000699361.1:n.322G>C
ENST00000699362.1:c.184G>C	ENSP00000514332.1:n.184G>C
ENST00000699363.1:c.184G>C	ENSP00000514333.1:n.184G>C
ENST00000699364.1:n.288G>C
ENST00000699365.1:c.357G>C	ENSP00000514334.1:p.Thr119=
ENST00000699366.1:n.111+1350G>C
ENST00000699367.1:n.112-1302G>C
ENST00000699368.1:c.775G>C	ENSP00000514335.1:n.775G>C
ENST00000525621.6:c.3288G>C MANE Select	ENSP00000431885.1:p.Thr1096=
ENST00000264818.10:c.3288G>C	ENSP00000264818.6:p.Thr1096=
ENST00000524462.5:c.2733G>C	ENSP00000433203.1:p.Thr911=
ENST00000525621.5:c.3288G>C	ENSP00000431885.1:p.Thr1096=
ENST00000525976.5:c.29G>C
ENST00000527481.2:c.465G>C
ENST00000529422.1:n.116+558G>C
ENST00000529739.1:c.357G>C	ENSP00000436155.1:p.Thr119=
ENST00000530220.1:n.331+462G>C
ENST00000530560.5:c.338-1496G>C	ENSP00000465291.1:n.338-1496G>C
ENST00000592137.1:n.442G>C
NM_003331.4:c.3288G>C , LRG_121t1:c.3288G>C	NP_003322.3:p.Thr1096=
XM_011528245.1:c.3288G>C	XP_011526547.1:p.Thr1096=
XM_011528246.1:c.2991G>C	XP_011526548.1:p.Thr997=
XM_011528247.1:c.2991G>C	XP_011526549.1:p.Thr997=
XM_011528248.1:c.3200+462G>C	XP_011526550.1:n.3200+462G>C
XM_011528249.1:c.1962G>C	XP_011526551.1:p.Thr654=
XM_011528251.1:c.1545G>C	XP_011526553.1:p.Thr515=
XM_011528246.3:c.2991G>C	XP_011526548.1:p.Thr997=
XM_011528249.2:c.1962G>C	XP_011526551.1:p.Thr654=
XR_001753750.1:n.3357+462G>C
XR_001753751.1:n.3840G>C
XR_002958353.1:n.4766G>C
NM_003331.5:c.3288G>C MANE Select	NP_003322.3:p.Thr1096=
NM_001385197.1:c.3288G>C	NP_001372126.1:p.Thr1096=
NM_001385198.1:c.3168+494G>C	NP_001372127.1:n.3168+494G>C
NM_001385199.1:c.3102G>C	NP_001372128.1:p.Thr1034=
NM_001385200.1:c.3285G>C	NP_001372129.1:p.Thr1095=
NM_001385201.1:c.3090G>C	NP_001372130.1:p.Thr1030=
NM_001385202.1:c.3204G>C	NP_001372131.1:p.Thr1068=
NM_001385203.1:c.3369G>C	NP_001372132.1:p.Thr1123=
NM_001385204.1:c.3498G>C	NP_001372133.1:p.Thr1166=
NM_001385205.1:c.3198G>C	NP_001372134.1:p.Thr1066=
NM_001385206.1:c.3162G>C	NP_001372135.1:p.Thr1054=
NM_001385207.1:c.3270G>C	NP_001372136.1:p.Thr1090=