Canonical Allele Identifier: CA403987791

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464750A>G (hg19) ; chr19:g.10354074A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354074A>G , CM000681.2:g.10354074A>G	GRCh38
NC_000019.9:g.10464750A>G , CM000681.1:g.10464750A>G	GRCh37
NC_000019.8:g.10325750A>G	NCBI36
NG_007872.1:g.31499T>C , LRG_121:g.31499T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1225T>C	ENSP00000514307.1:n.*1225T>C
ENST00000525976.6:c.2876T>C	ENSP00000434831.2:p.Ile959Thr
ENST00000527481.3:c.2876T>C	ENSP00000466340.2:p.Ile959Thr
ENST00000529370.6:n.4252T>C
ENST00000529739.2:n.3290T>C
ENST00000530829.2:c.*2427T>C	ENSP00000436826.2:n.*2427T>C
ENST00000531836.6:c.2876T>C	ENSP00000436175.2:p.Ile959Thr
ENST00000533334.2:c.*918T>C	ENSP00000432320.2:n.*918T>C
ENST00000534228.2:n.4335T>C
ENST00000699354.1:n.978T>C
ENST00000699355.1:c.*1981T>C	ENSP00000514328.1:n.*1981T>C
ENST00000699356.1:n.3290T>C
ENST00000699357.1:n.4335T>C
ENST00000699358.1:c.2876T>C	ENSP00000514329.1:p.Ile959Thr
ENST00000699359.1:c.82T>C
ENST00000699360.1:c.2876T>C	ENSP00000514331.1:p.Ile959Thr
ENST00000699368.1:c.80T>C	ENSP00000514335.1:p.Ile27Thr
ENST00000525621.6:c.2876T>C MANE Select	ENSP00000431885.1:p.Ile959Thr
ENST00000264818.10:c.2876T>C	ENSP00000264818.6:p.Ile959Thr
ENST00000524462.5:c.2321T>C	ENSP00000433203.1:p.Ile774Thr
ENST00000525621.5:c.2876T>C	ENSP00000431885.1:p.Ile959Thr
ENST00000527481.2:c.172T>C
ENST00000529412.1:n.548T>C
ENST00000529739.1:c.-451T>C	ENSP00000436155.1:n.-451T>C
ENST00000530560.5:c.305T>C	ENSP00000465291.1:p.Ile102Thr
ENST00000592137.1:n.30T>C
NM_003331.4:c.2876T>C , LRG_121t1:c.2876T>C	NP_003322.3:p.Ile959Thr
XM_011528245.1:c.2876T>C	XP_011526547.1:p.Ile959Thr
XM_011528246.1:c.2579T>C	XP_011526548.1:p.Ile860Thr
XM_011528247.1:c.2579T>C	XP_011526549.1:p.Ile860Thr
XM_011528248.1:c.2876T>C	XP_011526550.1:p.Ile959Thr
XM_011528249.1:c.1550T>C	XP_011526551.1:p.Ile517Thr
XM_011528251.1:c.1133T>C	XP_011526553.1:p.Ile378Thr
XM_011528246.3:c.2579T>C	XP_011526548.1:p.Ile860Thr
XM_011528249.2:c.1550T>C	XP_011526551.1:p.Ile517Thr
XR_001753750.1:n.3033T>C
XR_001753751.1:n.3033T>C
XR_002958353.1:n.3959T>C
NM_003331.5:c.2876T>C MANE Select	NP_003322.3:p.Ile959Thr
NM_001385197.1:c.2876T>C	NP_001372126.1:p.Ile959Thr
NM_001385198.1:c.2876T>C	NP_001372127.1:p.Ile959Thr
NM_001385199.1:c.2690T>C	NP_001372128.1:p.Ile897Thr
NM_001385200.1:c.2873T>C	NP_001372129.1:p.Ile958Thr
NM_001385201.1:c.2678T>C	NP_001372130.1:p.Ile893Thr
NM_001385202.1:c.2792T>C	NP_001372131.1:p.Ile931Thr
NM_001385203.1:c.2957T>C	NP_001372132.1:p.Ile986Thr
NM_001385204.1:c.3086T>C	NP_001372133.1:p.Ile1029Thr
NM_001385205.1:c.2786T>C	NP_001372134.1:p.Ile929Thr
NM_001385206.1:c.2750T>C	NP_001372135.1:p.Ile917Thr
NM_001385207.1:c.2858T>C	NP_001372136.1:p.Ile953Thr