Canonical Allele Identifier: CA403987741

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464744T>G (hg19) ; chr19:g.10354068T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354068T>G , CM000681.2:g.10354068T>G	GRCh38
NC_000019.9:g.10464744T>G , CM000681.1:g.10464744T>G	GRCh37
NC_000019.8:g.10325744T>G	NCBI36
NG_007872.1:g.31505A>C , LRG_121:g.31505A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1231A>C	ENSP00000514307.1:n.*1231A>C
ENST00000525976.6:c.2882A>C	ENSP00000434831.2:p.Lys961Thr
ENST00000527481.3:c.2882A>C	ENSP00000466340.2:p.Lys961Thr
ENST00000529370.6:n.4258A>C
ENST00000529739.2:n.3296A>C
ENST00000530829.2:c.*2433A>C	ENSP00000436826.2:n.*2433A>C
ENST00000531836.6:c.2882A>C	ENSP00000436175.2:p.Lys961Thr
ENST00000533334.2:c.*924A>C	ENSP00000432320.2:n.*924A>C
ENST00000534228.2:n.4341A>C
ENST00000699354.1:n.984A>C
ENST00000699355.1:c.*1987A>C	ENSP00000514328.1:n.*1987A>C
ENST00000699356.1:n.3296A>C
ENST00000699357.1:n.4341A>C
ENST00000699358.1:c.2882A>C	ENSP00000514329.1:p.Lys961Thr
ENST00000699359.1:c.88A>C
ENST00000699360.1:c.2882A>C	ENSP00000514331.1:p.Lys961Thr
ENST00000699368.1:c.86A>C	ENSP00000514335.1:p.Lys29Thr
ENST00000525621.6:c.2882A>C MANE Select	ENSP00000431885.1:p.Lys961Thr
ENST00000264818.10:c.2882A>C	ENSP00000264818.6:p.Lys961Thr
ENST00000524462.5:c.2327A>C	ENSP00000433203.1:p.Lys776Thr
ENST00000525621.5:c.2882A>C	ENSP00000431885.1:p.Lys961Thr
ENST00000527481.2:c.178A>C
ENST00000529412.1:n.554A>C
ENST00000529739.1:c.-445A>C	ENSP00000436155.1:n.-445A>C
ENST00000530560.5:c.311A>C	ENSP00000465291.1:p.Lys104Thr
ENST00000592137.1:n.36A>C
NM_003331.4:c.2882A>C , LRG_121t1:c.2882A>C	NP_003322.3:p.Lys961Thr
XM_011528245.1:c.2882A>C	XP_011526547.1:p.Lys961Thr
XM_011528246.1:c.2585A>C	XP_011526548.1:p.Lys862Thr
XM_011528247.1:c.2585A>C	XP_011526549.1:p.Lys862Thr
XM_011528248.1:c.2882A>C	XP_011526550.1:p.Lys961Thr
XM_011528249.1:c.1556A>C	XP_011526551.1:p.Lys519Thr
XM_011528251.1:c.1139A>C	XP_011526553.1:p.Lys380Thr
XM_011528246.3:c.2585A>C	XP_011526548.1:p.Lys862Thr
XM_011528249.2:c.1556A>C	XP_011526551.1:p.Lys519Thr
XR_001753750.1:n.3039A>C
XR_001753751.1:n.3039A>C
XR_002958353.1:n.3965A>C
NM_003331.5:c.2882A>C MANE Select	NP_003322.3:p.Lys961Thr
NM_001385197.1:c.2882A>C	NP_001372126.1:p.Lys961Thr
NM_001385198.1:c.2882A>C	NP_001372127.1:p.Lys961Thr
NM_001385199.1:c.2696A>C	NP_001372128.1:p.Lys899Thr
NM_001385200.1:c.2879A>C	NP_001372129.1:p.Lys960Thr
NM_001385201.1:c.2684A>C	NP_001372130.1:p.Lys895Thr
NM_001385202.1:c.2798A>C	NP_001372131.1:p.Lys933Thr
NM_001385203.1:c.2963A>C	NP_001372132.1:p.Lys988Thr
NM_001385204.1:c.3092A>C	NP_001372133.1:p.Lys1031Thr
NM_001385205.1:c.2792A>C	NP_001372134.1:p.Lys931Thr
NM_001385206.1:c.2756A>C	NP_001372135.1:p.Lys919Thr
NM_001385207.1:c.2864A>C	NP_001372136.1:p.Lys955Thr