Canonical Allele Identifier: CA505373981

Gene: TYK2

Linked Data

• gnomAD v4: 19-10354166-C-T
• MyVariant Identifiers: chr19:g.10464842C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354166C>T , CM000681.2:g.10354166C>T	GRCh38
NC_000019.9:g.10464842C>T , CM000681.1:g.10464842C>T	GRCh37
NC_000019.8:g.10325842C>T	NCBI36
NG_007872.1:g.31407G>A , LRG_121:g.31407G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1133G>A	ENSP00000514307.1:n.*1133G>A
ENST00000525976.6:c.2784G>A	ENSP00000434831.2:p.Ala928=
ENST00000527481.3:c.2784G>A	ENSP00000466340.2:p.Ala928=
ENST00000529370.6:n.4160G>A
ENST00000529739.2:n.3198G>A
ENST00000530829.2:c.*2335G>A	ENSP00000436826.2:n.*2335G>A
ENST00000531836.6:c.2784G>A	ENSP00000436175.2:p.Ala928=
ENST00000533334.2:c.*826G>A	ENSP00000432320.2:n.*826G>A
ENST00000534228.2:n.4243G>A
ENST00000699354.1:n.886G>A
ENST00000699355.1:c.*1889G>A	ENSP00000514328.1:n.*1889G>A
ENST00000699356.1:n.3198G>A
ENST00000699357.1:n.4243G>A
ENST00000699358.1:c.2784G>A	ENSP00000514329.1:p.Ala928=
ENST00000699360.1:c.2784G>A	ENSP00000514331.1:p.Ala928=
ENST00000525621.6:c.2784G>A MANE Select	ENSP00000431885.1:p.Ala928=
ENST00000264818.10:c.2784G>A	ENSP00000264818.6:p.Ala928=
ENST00000524462.5:c.2229G>A	ENSP00000433203.1:p.Ala743=
ENST00000525621.5:c.2784G>A	ENSP00000431885.1:p.Ala928=
ENST00000527481.2:c.80G>A
ENST00000529412.1:n.456G>A
ENST00000530560.5:c.213G>A	ENSP00000465291.1:p.Ala71=
NM_003331.4:c.2784G>A , LRG_121t1:c.2784G>A	NP_003322.3:p.Ala928=
XM_011528245.1:c.2784G>A	XP_011526547.1:p.Ala928=
XM_011528246.1:c.2487G>A	XP_011526548.1:p.Ala829=
XM_011528247.1:c.2487G>A	XP_011526549.1:p.Ala829=
XM_011528248.1:c.2784G>A	XP_011526550.1:p.Ala928=
XM_011528249.1:c.1458G>A	XP_011526551.1:p.Ala486=
XM_011528251.1:c.1041G>A	XP_011526553.1:p.Ala347=
XM_011528246.3:c.2487G>A	XP_011526548.1:p.Ala829=
XM_011528249.2:c.1458G>A	XP_011526551.1:p.Ala486=
XR_001753750.1:n.2941G>A
XR_001753751.1:n.2941G>A
XR_002958353.1:n.3867G>A
NM_003331.5:c.2784G>A MANE Select	NP_003322.3:p.Ala928=
NM_001385197.1:c.2784G>A	NP_001372126.1:p.Ala928=
NM_001385198.1:c.2784G>A	NP_001372127.1:p.Ala928=
NM_001385199.1:c.2598G>A	NP_001372128.1:p.Ala866=
NM_001385200.1:c.2781G>A	NP_001372129.1:p.Ala927=
NM_001385201.1:c.2586G>A	NP_001372130.1:p.Ala862=
NM_001385202.1:c.2700G>A	NP_001372131.1:p.Ala900=
NM_001385203.1:c.2865G>A	NP_001372132.1:p.Ala955=
NM_001385204.1:c.2994G>A	NP_001372133.1:p.Ala998=
NM_001385205.1:c.2694G>A	NP_001372134.1:p.Ala898=
NM_001385206.1:c.2658G>A	NP_001372135.1:p.Ala886=
NM_001385207.1:c.2766G>A	NP_001372136.1:p.Ala922=