Canonical Allele Identifier: CA505373895

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464824T>C (hg19)

Genomic Alleles

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

Transcript Alleles

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