Canonical Allele Identifier: CA403987712

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464742A>T (hg19) ; chr19:g.10354066A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354066A>T , CM000681.2:g.10354066A>T	GRCh38
NC_000019.9:g.10464742A>T , CM000681.1:g.10464742A>T	GRCh37
NC_000019.8:g.10325742A>T	NCBI36
NG_007872.1:g.31507T>A , LRG_121:g.31507T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1233T>A	ENSP00000514307.1:n.*1233T>A
ENST00000525976.6:c.2884T>A	ENSP00000434831.2:p.Tyr962Asn
ENST00000527481.3:c.2884T>A	ENSP00000466340.2:p.Tyr962Asn
ENST00000529370.6:n.4260T>A
ENST00000529739.2:n.3298T>A
ENST00000530829.2:c.*2435T>A	ENSP00000436826.2:n.*2435T>A
ENST00000531836.6:c.2884T>A	ENSP00000436175.2:p.Tyr962Asn
ENST00000533334.2:c.*926T>A	ENSP00000432320.2:n.*926T>A
ENST00000534228.2:n.4343T>A
ENST00000699354.1:n.986T>A
ENST00000699355.1:c.*1989T>A	ENSP00000514328.1:n.*1989T>A
ENST00000699356.1:n.3298T>A
ENST00000699357.1:n.4343T>A
ENST00000699358.1:c.2884T>A	ENSP00000514329.1:p.Tyr962Asn
ENST00000699359.1:c.90T>A
ENST00000699360.1:c.2884T>A	ENSP00000514331.1:p.Tyr962Asn
ENST00000699368.1:c.88T>A	ENSP00000514335.1:p.Tyr30Asn
ENST00000525621.6:c.2884T>A MANE Select	ENSP00000431885.1:p.Tyr962Asn
ENST00000264818.10:c.2884T>A	ENSP00000264818.6:p.Tyr962Asn
ENST00000524462.5:c.2329T>A	ENSP00000433203.1:p.Tyr777Asn
ENST00000525621.5:c.2884T>A	ENSP00000431885.1:p.Tyr962Asn
ENST00000527481.2:c.180T>A
ENST00000529412.1:n.556T>A
ENST00000529739.1:c.-443T>A	ENSP00000436155.1:n.-443T>A
ENST00000530560.5:c.313T>A	ENSP00000465291.1:p.Tyr105Asn
ENST00000592137.1:n.38T>A
NM_003331.4:c.2884T>A , LRG_121t1:c.2884T>A	NP_003322.3:p.Tyr962Asn
XM_011528245.1:c.2884T>A	XP_011526547.1:p.Tyr962Asn
XM_011528246.1:c.2587T>A	XP_011526548.1:p.Tyr863Asn
XM_011528247.1:c.2587T>A	XP_011526549.1:p.Tyr863Asn
XM_011528248.1:c.2884T>A	XP_011526550.1:p.Tyr962Asn
XM_011528249.1:c.1558T>A	XP_011526551.1:p.Tyr520Asn
XM_011528251.1:c.1141T>A	XP_011526553.1:p.Tyr381Asn
XM_011528246.3:c.2587T>A	XP_011526548.1:p.Tyr863Asn
XM_011528249.2:c.1558T>A	XP_011526551.1:p.Tyr520Asn
XR_001753750.1:n.3041T>A
XR_001753751.1:n.3041T>A
XR_002958353.1:n.3967T>A
NM_003331.5:c.2884T>A MANE Select	NP_003322.3:p.Tyr962Asn
NM_001385197.1:c.2884T>A	NP_001372126.1:p.Tyr962Asn
NM_001385198.1:c.2884T>A	NP_001372127.1:p.Tyr962Asn
NM_001385199.1:c.2698T>A	NP_001372128.1:p.Tyr900Asn
NM_001385200.1:c.2881T>A	NP_001372129.1:p.Tyr961Asn
NM_001385201.1:c.2686T>A	NP_001372130.1:p.Tyr896Asn
NM_001385202.1:c.2800T>A	NP_001372131.1:p.Tyr934Asn
NM_001385203.1:c.2965T>A	NP_001372132.1:p.Tyr989Asn
NM_001385204.1:c.3094T>A	NP_001372133.1:p.Tyr1032Asn
NM_001385205.1:c.2794T>A	NP_001372134.1:p.Tyr932Asn
NM_001385206.1:c.2758T>A	NP_001372135.1:p.Tyr920Asn
NM_001385207.1:c.2866T>A	NP_001372136.1:p.Tyr956Asn