Canonical Allele Identifier: CA403988518

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464825G>A (hg19) ; chr19:g.10354149G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354149G>A , CM000681.2:g.10354149G>A	GRCh38
NC_000019.9:g.10464825G>A , CM000681.1:g.10464825G>A	GRCh37
NC_000019.8:g.10325825G>A	NCBI36
NG_007872.1:g.31424C>T , LRG_121:g.31424C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1150C>T	ENSP00000514307.1:n.*1150C>T
ENST00000525976.6:c.2801C>T	ENSP00000434831.2:p.Ala934Val
ENST00000527481.3:c.2801C>T	ENSP00000466340.2:p.Ala934Val
ENST00000529370.6:n.4177C>T
ENST00000529739.2:n.3215C>T
ENST00000530829.2:c.*2352C>T	ENSP00000436826.2:n.*2352C>T
ENST00000531836.6:c.2801C>T	ENSP00000436175.2:p.Ala934Val
ENST00000533334.2:c.*843C>T	ENSP00000432320.2:n.*843C>T
ENST00000534228.2:n.4260C>T
ENST00000699354.1:n.903C>T
ENST00000699355.1:c.*1906C>T	ENSP00000514328.1:n.*1906C>T
ENST00000699356.1:n.3215C>T
ENST00000699357.1:n.4260C>T
ENST00000699358.1:c.2801C>T	ENSP00000514329.1:p.Ala934Val
ENST00000699359.1:c.7C>T
ENST00000699360.1:c.2801C>T	ENSP00000514331.1:p.Ala934Val
ENST00000699368.1:c.5C>T	ENSP00000514335.1:p.Ala2Val
ENST00000525621.6:c.2801C>T MANE Select	ENSP00000431885.1:p.Ala934Val
ENST00000264818.10:c.2801C>T	ENSP00000264818.6:p.Ala934Val
ENST00000524462.5:c.2246C>T	ENSP00000433203.1:p.Ala749Val
ENST00000525621.5:c.2801C>T	ENSP00000431885.1:p.Ala934Val
ENST00000527481.2:c.97C>T
ENST00000529412.1:n.473C>T
ENST00000530560.5:c.230C>T	ENSP00000465291.1:p.Ala77Val
NM_003331.4:c.2801C>T , LRG_121t1:c.2801C>T	NP_003322.3:p.Ala934Val
XM_011528245.1:c.2801C>T	XP_011526547.1:p.Ala934Val
XM_011528246.1:c.2504C>T	XP_011526548.1:p.Ala835Val
XM_011528247.1:c.2504C>T	XP_011526549.1:p.Ala835Val
XM_011528248.1:c.2801C>T	XP_011526550.1:p.Ala934Val
XM_011528249.1:c.1475C>T	XP_011526551.1:p.Ala492Val
XM_011528251.1:c.1058C>T	XP_011526553.1:p.Ala353Val
XM_011528246.3:c.2504C>T	XP_011526548.1:p.Ala835Val
XM_011528249.2:c.1475C>T	XP_011526551.1:p.Ala492Val
XR_001753750.1:n.2958C>T
XR_001753751.1:n.2958C>T
XR_002958353.1:n.3884C>T
NM_003331.5:c.2801C>T MANE Select	NP_003322.3:p.Ala934Val
NM_001385197.1:c.2801C>T	NP_001372126.1:p.Ala934Val
NM_001385198.1:c.2801C>T	NP_001372127.1:p.Ala934Val
NM_001385199.1:c.2615C>T	NP_001372128.1:p.Ala872Val
NM_001385200.1:c.2798C>T	NP_001372129.1:p.Ala933Val
NM_001385201.1:c.2603C>T	NP_001372130.1:p.Ala868Val
NM_001385202.1:c.2717C>T	NP_001372131.1:p.Ala906Val
NM_001385203.1:c.2882C>T	NP_001372132.1:p.Ala961Val
NM_001385204.1:c.3011C>T	NP_001372133.1:p.Ala1004Val
NM_001385205.1:c.2711C>T	NP_001372134.1:p.Ala904Val
NM_001385206.1:c.2675C>T	NP_001372135.1:p.Ala892Val
NM_001385207.1:c.2783C>T	NP_001372136.1:p.Ala928Val