Canonical Allele Identifier: CA505373894

Gene: TYK2

Linked Data

• gnomAD v4: 19-10354148-T-A
• MyVariant Identifiers: chr19:g.10464824T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354148T>A , CM000681.2:g.10354148T>A	GRCh38
NC_000019.9:g.10464824T>A , CM000681.1:g.10464824T>A	GRCh37
NC_000019.8:g.10325824T>A	NCBI36
NG_007872.1:g.31425A>T , LRG_121:g.31425A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1151A>T	ENSP00000514307.1:n.*1151A>T
ENST00000525976.6:c.2802A>T	ENSP00000434831.2:p.Ala934=
ENST00000527481.3:c.2802A>T	ENSP00000466340.2:p.Ala934=
ENST00000529370.6:n.4178A>T
ENST00000529739.2:n.3216A>T
ENST00000530829.2:c.*2353A>T	ENSP00000436826.2:n.*2353A>T
ENST00000531836.6:c.2802A>T	ENSP00000436175.2:p.Ala934=
ENST00000533334.2:c.*844A>T	ENSP00000432320.2:n.*844A>T
ENST00000534228.2:n.4261A>T
ENST00000699354.1:n.904A>T
ENST00000699355.1:c.*1907A>T	ENSP00000514328.1:n.*1907A>T
ENST00000699356.1:n.3216A>T
ENST00000699357.1:n.4261A>T
ENST00000699358.1:c.2802A>T	ENSP00000514329.1:p.Ala934=
ENST00000699359.1:c.8A>T
ENST00000699360.1:c.2802A>T	ENSP00000514331.1:p.Ala934=
ENST00000699368.1:c.6A>T	ENSP00000514335.1:p.Ala2=
ENST00000525621.6:c.2802A>T MANE Select	ENSP00000431885.1:p.Ala934=
ENST00000264818.10:c.2802A>T	ENSP00000264818.6:p.Ala934=
ENST00000524462.5:c.2247A>T	ENSP00000433203.1:p.Ala749=
ENST00000525621.5:c.2802A>T	ENSP00000431885.1:p.Ala934=
ENST00000527481.2:c.98A>T
ENST00000529412.1:n.474A>T
ENST00000530560.5:c.231A>T	ENSP00000465291.1:p.Ala77=
NM_003331.4:c.2802A>T , LRG_121t1:c.2802A>T	NP_003322.3:p.Ala934=
XM_011528245.1:c.2802A>T	XP_011526547.1:p.Ala934=
XM_011528246.1:c.2505A>T	XP_011526548.1:p.Ala835=
XM_011528247.1:c.2505A>T	XP_011526549.1:p.Ala835=
XM_011528248.1:c.2802A>T	XP_011526550.1:p.Ala934=
XM_011528249.1:c.1476A>T	XP_011526551.1:p.Ala492=
XM_011528251.1:c.1059A>T	XP_011526553.1:p.Ala353=
XM_011528246.3:c.2505A>T	XP_011526548.1:p.Ala835=
XM_011528249.2:c.1476A>T	XP_011526551.1:p.Ala492=
XR_001753750.1:n.2959A>T
XR_001753751.1:n.2959A>T
XR_002958353.1:n.3885A>T
NM_003331.5:c.2802A>T MANE Select	NP_003322.3:p.Ala934=
NM_001385197.1:c.2802A>T	NP_001372126.1:p.Ala934=
NM_001385198.1:c.2802A>T	NP_001372127.1:p.Ala934=
NM_001385199.1:c.2616A>T	NP_001372128.1:p.Ala872=
NM_001385200.1:c.2799A>T	NP_001372129.1:p.Ala933=
NM_001385201.1:c.2604A>T	NP_001372130.1:p.Ala868=
NM_001385202.1:c.2718A>T	NP_001372131.1:p.Ala906=
NM_001385203.1:c.2883A>T	NP_001372132.1:p.Ala961=
NM_001385204.1:c.3012A>T	NP_001372133.1:p.Ala1004=
NM_001385205.1:c.2712A>T	NP_001372134.1:p.Ala904=
NM_001385206.1:c.2676A>T	NP_001372135.1:p.Ala892=
NM_001385207.1:c.2784A>T	NP_001372136.1:p.Ala928=