Canonical Allele Identifier: CA505373868

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464815G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354139G>T , CM000681.2:g.10354139G>T	GRCh38
NC_000019.9:g.10464815G>T , CM000681.1:g.10464815G>T	GRCh37
NC_000019.8:g.10325815G>T	NCBI36
NG_007872.1:g.31434C>A , LRG_121:g.31434C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1160C>A	ENSP00000514307.1:n.*1160C>A
ENST00000525976.6:c.2811C>A	ENSP00000434831.2:p.Gly937=
ENST00000527481.3:c.2811C>A	ENSP00000466340.2:p.Gly937=
ENST00000529370.6:n.4187C>A
ENST00000529739.2:n.3225C>A
ENST00000530829.2:c.*2362C>A	ENSP00000436826.2:n.*2362C>A
ENST00000531836.6:c.2811C>A	ENSP00000436175.2:p.Gly937=
ENST00000533334.2:c.*853C>A	ENSP00000432320.2:n.*853C>A
ENST00000534228.2:n.4270C>A
ENST00000699354.1:n.913C>A
ENST00000699355.1:c.*1916C>A	ENSP00000514328.1:n.*1916C>A
ENST00000699356.1:n.3225C>A
ENST00000699357.1:n.4270C>A
ENST00000699358.1:c.2811C>A	ENSP00000514329.1:p.Gly937=
ENST00000699359.1:c.17C>A
ENST00000699360.1:c.2811C>A	ENSP00000514331.1:p.Gly937=
ENST00000699368.1:c.15C>A	ENSP00000514335.1:p.Gly5=
ENST00000525621.6:c.2811C>A MANE Select	ENSP00000431885.1:p.Gly937=
ENST00000264818.10:c.2811C>A	ENSP00000264818.6:p.Gly937=
ENST00000524462.5:c.2256C>A	ENSP00000433203.1:p.Gly752=
ENST00000525621.5:c.2811C>A	ENSP00000431885.1:p.Gly937=
ENST00000527481.2:c.107C>A
ENST00000529412.1:n.483C>A
ENST00000530560.5:c.240C>A	ENSP00000465291.1:p.Gly80=
NM_003331.4:c.2811C>A , LRG_121t1:c.2811C>A	NP_003322.3:p.Gly937=
XM_011528245.1:c.2811C>A	XP_011526547.1:p.Gly937=
XM_011528246.1:c.2514C>A	XP_011526548.1:p.Gly838=
XM_011528247.1:c.2514C>A	XP_011526549.1:p.Gly838=
XM_011528248.1:c.2811C>A	XP_011526550.1:p.Gly937=
XM_011528249.1:c.1485C>A	XP_011526551.1:p.Gly495=
XM_011528251.1:c.1068C>A	XP_011526553.1:p.Gly356=
XM_011528246.3:c.2514C>A	XP_011526548.1:p.Gly838=
XM_011528249.2:c.1485C>A	XP_011526551.1:p.Gly495=
XR_001753750.1:n.2968C>A
XR_001753751.1:n.2968C>A
XR_002958353.1:n.3894C>A
NM_003331.5:c.2811C>A MANE Select	NP_003322.3:p.Gly937=
NM_001385197.1:c.2811C>A	NP_001372126.1:p.Gly937=
NM_001385198.1:c.2811C>A	NP_001372127.1:p.Gly937=
NM_001385199.1:c.2625C>A	NP_001372128.1:p.Gly875=
NM_001385200.1:c.2808C>A	NP_001372129.1:p.Gly936=
NM_001385201.1:c.2613C>A	NP_001372130.1:p.Gly871=
NM_001385202.1:c.2727C>A	NP_001372131.1:p.Gly909=
NM_001385203.1:c.2892C>A	NP_001372132.1:p.Gly964=
NM_001385204.1:c.3021C>A	NP_001372133.1:p.Gly1007=
NM_001385205.1:c.2721C>A	NP_001372134.1:p.Gly907=
NM_001385206.1:c.2685C>A	NP_001372135.1:p.Gly895=
NM_001385207.1:c.2793C>A	NP_001372136.1:p.Gly931=