Canonical Allele Identifier: CA403988050

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464783A>T (hg19) ; chr19:g.10354107A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354107A>T , CM000681.2:g.10354107A>T	GRCh38
NC_000019.9:g.10464783A>T , CM000681.1:g.10464783A>T	GRCh37
NC_000019.8:g.10325783A>T	NCBI36
NG_007872.1:g.31466T>A , LRG_121:g.31466T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1192T>A	ENSP00000514307.1:n.*1192T>A
ENST00000525976.6:c.2843T>A	ENSP00000434831.2:p.Ile948Asn
ENST00000527481.3:c.2843T>A	ENSP00000466340.2:p.Ile948Asn
ENST00000529370.6:n.4219T>A
ENST00000529739.2:n.3257T>A
ENST00000530829.2:c.*2394T>A	ENSP00000436826.2:n.*2394T>A
ENST00000531836.6:c.2843T>A	ENSP00000436175.2:p.Ile948Asn
ENST00000533334.2:c.*885T>A	ENSP00000432320.2:n.*885T>A
ENST00000534228.2:n.4302T>A
ENST00000699354.1:n.945T>A
ENST00000699355.1:c.*1948T>A	ENSP00000514328.1:n.*1948T>A
ENST00000699356.1:n.3257T>A
ENST00000699357.1:n.4302T>A
ENST00000699358.1:c.2843T>A	ENSP00000514329.1:p.Ile948Asn
ENST00000699359.1:c.49T>A
ENST00000699360.1:c.2843T>A	ENSP00000514331.1:p.Ile948Asn
ENST00000699368.1:c.47T>A	ENSP00000514335.1:p.Ile16Asn
ENST00000525621.6:c.2843T>A MANE Select	ENSP00000431885.1:p.Ile948Asn
ENST00000264818.10:c.2843T>A	ENSP00000264818.6:p.Ile948Asn
ENST00000524462.5:c.2288T>A	ENSP00000433203.1:p.Ile763Asn
ENST00000525621.5:c.2843T>A	ENSP00000431885.1:p.Ile948Asn
ENST00000527481.2:c.139T>A
ENST00000529412.1:n.515T>A
ENST00000530560.5:c.272T>A	ENSP00000465291.1:p.Ile91Asn
NM_003331.4:c.2843T>A , LRG_121t1:c.2843T>A	NP_003322.3:p.Ile948Asn
XM_011528245.1:c.2843T>A	XP_011526547.1:p.Ile948Asn
XM_011528246.1:c.2546T>A	XP_011526548.1:p.Ile849Asn
XM_011528247.1:c.2546T>A	XP_011526549.1:p.Ile849Asn
XM_011528248.1:c.2843T>A	XP_011526550.1:p.Ile948Asn
XM_011528249.1:c.1517T>A	XP_011526551.1:p.Ile506Asn
XM_011528251.1:c.1100T>A	XP_011526553.1:p.Ile367Asn
XM_011528246.3:c.2546T>A	XP_011526548.1:p.Ile849Asn
XM_011528249.2:c.1517T>A	XP_011526551.1:p.Ile506Asn
XR_001753750.1:n.3000T>A
XR_001753751.1:n.3000T>A
XR_002958353.1:n.3926T>A
NM_003331.5:c.2843T>A MANE Select	NP_003322.3:p.Ile948Asn
NM_001385197.1:c.2843T>A	NP_001372126.1:p.Ile948Asn
NM_001385198.1:c.2843T>A	NP_001372127.1:p.Ile948Asn
NM_001385199.1:c.2657T>A	NP_001372128.1:p.Ile886Asn
NM_001385200.1:c.2840T>A	NP_001372129.1:p.Ile947Asn
NM_001385201.1:c.2645T>A	NP_001372130.1:p.Ile882Asn
NM_001385202.1:c.2759T>A	NP_001372131.1:p.Ile920Asn
NM_001385203.1:c.2924T>A	NP_001372132.1:p.Ile975Asn
NM_001385204.1:c.3053T>A	NP_001372133.1:p.Ile1018Asn
NM_001385205.1:c.2753T>A	NP_001372134.1:p.Ile918Asn
NM_001385206.1:c.2717T>A	NP_001372135.1:p.Ile906Asn
NM_001385207.1:c.2825T>A	NP_001372136.1:p.Ile942Asn