Canonical Allele Identifier: CA403989349

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464905G>C (hg19) ; chr19:g.10354229G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354229G>C , CM000681.2:g.10354229G>C	GRCh38
NC_000019.9:g.10464905G>C , CM000681.1:g.10464905G>C	GRCh37
NC_000019.8:g.10325905G>C	NCBI36
NG_007872.1:g.31344C>G , LRG_121:g.31344C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1070C>G	ENSP00000514307.1:n.*1070C>G
ENST00000525976.6:c.2721C>G	ENSP00000434831.2:p.His907Gln
ENST00000527481.3:c.2721C>G	ENSP00000466340.2:p.His907Gln
ENST00000529370.6:n.4097C>G
ENST00000529739.2:n.3135C>G
ENST00000530829.2:c.*2272C>G	ENSP00000436826.2:n.*2272C>G
ENST00000531836.6:c.2721C>G	ENSP00000436175.2:p.His907Gln
ENST00000533334.2:c.*763C>G	ENSP00000432320.2:n.*763C>G
ENST00000534228.2:n.4180C>G
ENST00000699354.1:n.823C>G
ENST00000699355.1:c.*1826C>G	ENSP00000514328.1:n.*1826C>G
ENST00000699356.1:n.3135C>G
ENST00000699357.1:n.4180C>G
ENST00000699358.1:c.2721C>G	ENSP00000514329.1:p.His907Gln
ENST00000699360.1:c.2721C>G	ENSP00000514331.1:p.His907Gln
ENST00000525621.6:c.2721C>G MANE Select	ENSP00000431885.1:p.His907Gln
ENST00000264818.10:c.2721C>G	ENSP00000264818.6:p.His907Gln
ENST00000524462.5:c.2166C>G	ENSP00000433203.1:p.His722Gln
ENST00000525621.5:c.2721C>G	ENSP00000431885.1:p.His907Gln
ENST00000527481.2:c.17C>G
ENST00000529412.1:n.393C>G
ENST00000530560.5:c.150C>G	ENSP00000465291.1:p.His50Gln
NM_003331.4:c.2721C>G , LRG_121t1:c.2721C>G	NP_003322.3:p.His907Gln
XM_011528245.1:c.2721C>G	XP_011526547.1:p.His907Gln
XM_011528246.1:c.2424C>G	XP_011526548.1:p.His808Gln
XM_011528247.1:c.2424C>G	XP_011526549.1:p.His808Gln
XM_011528248.1:c.2721C>G	XP_011526550.1:p.His907Gln
XM_011528249.1:c.1395C>G	XP_011526551.1:p.His465Gln
XM_011528251.1:c.978C>G	XP_011526553.1:p.His326Gln
XM_011528246.3:c.2424C>G	XP_011526548.1:p.His808Gln
XM_011528249.2:c.1395C>G	XP_011526551.1:p.His465Gln
XR_001753750.1:n.2878C>G
XR_001753751.1:n.2878C>G
XR_002958353.1:n.3804C>G
NM_003331.5:c.2721C>G MANE Select	NP_003322.3:p.His907Gln
NM_001385197.1:c.2721C>G	NP_001372126.1:p.His907Gln
NM_001385198.1:c.2721C>G	NP_001372127.1:p.His907Gln
NM_001385199.1:c.2535C>G	NP_001372128.1:p.His845Gln
NM_001385200.1:c.2718C>G	NP_001372129.1:p.His906Gln
NM_001385201.1:c.2523C>G	NP_001372130.1:p.His841Gln
NM_001385202.1:c.2637C>G	NP_001372131.1:p.His879Gln
NM_001385203.1:c.2802C>G	NP_001372132.1:p.His934Gln
NM_001385204.1:c.2931C>G	NP_001372133.1:p.His977Gln
NM_001385205.1:c.2631C>G	NP_001372134.1:p.His877Gln
NM_001385206.1:c.2595C>G	NP_001372135.1:p.His865Gln
NM_001385207.1:c.2703C>G	NP_001372136.1:p.His901Gln