Canonical Allele Identifier: CA505373908

Gene: TYK2

Linked Data

• dbSNP Id: rs1314804989
• gnomAD v2: 19-10464827-C-T
• gnomAD v4: 19-10354151-C-T
• MyVariant Identifiers: chr19:g.10464827C>T (hg19) ; chr19:g.10354151C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354151C>T , CM000681.2:g.10354151C>T	GRCh38
NC_000019.9:g.10464827C>T , CM000681.1:g.10464827C>T	GRCh37
NC_000019.8:g.10325827C>T	NCBI36
NG_007872.1:g.31422G>A , LRG_121:g.31422G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1148G>A	ENSP00000514307.1:n.*1148G>A
ENST00000525976.6:c.2799G>A	ENSP00000434831.2:p.Lys933=
ENST00000527481.3:c.2799G>A	ENSP00000466340.2:p.Lys933=
ENST00000529370.6:n.4175G>A
ENST00000529739.2:n.3213G>A
ENST00000530829.2:c.*2350G>A	ENSP00000436826.2:n.*2350G>A
ENST00000531836.6:c.2799G>A	ENSP00000436175.2:p.Lys933=
ENST00000533334.2:c.*841G>A	ENSP00000432320.2:n.*841G>A
ENST00000534228.2:n.4258G>A
ENST00000699354.1:n.901G>A
ENST00000699355.1:c.*1904G>A	ENSP00000514328.1:n.*1904G>A
ENST00000699356.1:n.3213G>A
ENST00000699357.1:n.4258G>A
ENST00000699358.1:c.2799G>A	ENSP00000514329.1:p.Lys933=
ENST00000699359.1:c.5G>A
ENST00000699360.1:c.2799G>A	ENSP00000514331.1:p.Lys933=
ENST00000699368.1:c.3G>A	ENSP00000514335.1:p.Lys1=
ENST00000525621.6:c.2799G>A MANE Select	ENSP00000431885.1:p.Lys933=
ENST00000264818.10:c.2799G>A	ENSP00000264818.6:p.Lys933=
ENST00000524462.5:c.2244G>A	ENSP00000433203.1:p.Lys748=
ENST00000525621.5:c.2799G>A	ENSP00000431885.1:p.Lys933=
ENST00000527481.2:c.95G>A
ENST00000529412.1:n.471G>A
ENST00000530560.5:c.228G>A	ENSP00000465291.1:p.Lys76=
NM_003331.4:c.2799G>A , LRG_121t1:c.2799G>A	NP_003322.3:p.Lys933=
XM_011528245.1:c.2799G>A	XP_011526547.1:p.Lys933=
XM_011528246.1:c.2502G>A	XP_011526548.1:p.Lys834=
XM_011528247.1:c.2502G>A	XP_011526549.1:p.Lys834=
XM_011528248.1:c.2799G>A	XP_011526550.1:p.Lys933=
XM_011528249.1:c.1473G>A	XP_011526551.1:p.Lys491=
XM_011528251.1:c.1056G>A	XP_011526553.1:p.Lys352=
XM_011528246.3:c.2502G>A	XP_011526548.1:p.Lys834=
XM_011528249.2:c.1473G>A	XP_011526551.1:p.Lys491=
XR_001753750.1:n.2956G>A
XR_001753751.1:n.2956G>A
XR_002958353.1:n.3882G>A
NM_003331.5:c.2799G>A MANE Select	NP_003322.3:p.Lys933=
NM_001385197.1:c.2799G>A	NP_001372126.1:p.Lys933=
NM_001385198.1:c.2799G>A	NP_001372127.1:p.Lys933=
NM_001385199.1:c.2613G>A	NP_001372128.1:p.Lys871=
NM_001385200.1:c.2796G>A	NP_001372129.1:p.Lys932=
NM_001385201.1:c.2601G>A	NP_001372130.1:p.Lys867=
NM_001385202.1:c.2715G>A	NP_001372131.1:p.Lys905=
NM_001385203.1:c.2880G>A	NP_001372132.1:p.Lys960=
NM_001385204.1:c.3009G>A	NP_001372133.1:p.Lys1003=
NM_001385205.1:c.2709G>A	NP_001372134.1:p.Lys903=
NM_001385206.1:c.2673G>A	NP_001372135.1:p.Lys891=
NM_001385207.1:c.2781G>A	NP_001372136.1:p.Lys927=