Canonical Allele Identifier: CA403988904

Gene: TYK2

Linked Data

• dbSNP Id: rs2040963961
• gnomAD v4: 19-10354189-C-T
• MyVariant Identifiers: chr19:g.10464865C>T (hg19) ; chr19:g.10354189C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354189C>T , CM000681.2:g.10354189C>T	GRCh38
NC_000019.9:g.10464865C>T , CM000681.1:g.10464865C>T	GRCh37
NC_000019.8:g.10325865C>T	NCBI36
NG_007872.1:g.31384G>A , LRG_121:g.31384G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1110G>A	ENSP00000514307.1:n.*1110G>A
ENST00000525976.6:c.2761G>A	ENSP00000434831.2:p.Asp921Asn
ENST00000527481.3:c.2761G>A	ENSP00000466340.2:p.Asp921Asn
ENST00000529370.6:n.4137G>A
ENST00000529739.2:n.3175G>A
ENST00000530829.2:c.*2312G>A	ENSP00000436826.2:n.*2312G>A
ENST00000531836.6:c.2761G>A	ENSP00000436175.2:p.Asp921Asn
ENST00000533334.2:c.*803G>A	ENSP00000432320.2:n.*803G>A
ENST00000534228.2:n.4220G>A
ENST00000699354.1:n.863G>A
ENST00000699355.1:c.*1866G>A	ENSP00000514328.1:n.*1866G>A
ENST00000699356.1:n.3175G>A
ENST00000699357.1:n.4220G>A
ENST00000699358.1:c.2761G>A	ENSP00000514329.1:p.Asp921Asn
ENST00000699360.1:c.2761G>A	ENSP00000514331.1:p.Asp921Asn
ENST00000525621.6:c.2761G>A MANE Select	ENSP00000431885.1:p.Asp921Asn
ENST00000264818.10:c.2761G>A	ENSP00000264818.6:p.Asp921Asn
ENST00000524462.5:c.2206G>A	ENSP00000433203.1:p.Asp736Asn
ENST00000525621.5:c.2761G>A	ENSP00000431885.1:p.Asp921Asn
ENST00000527481.2:c.57G>A
ENST00000529412.1:n.433G>A
ENST00000530560.5:c.190G>A	ENSP00000465291.1:p.Asp64Asn
NM_003331.4:c.2761G>A , LRG_121t1:c.2761G>A	NP_003322.3:p.Asp921Asn
XM_011528245.1:c.2761G>A	XP_011526547.1:p.Asp921Asn
XM_011528246.1:c.2464G>A	XP_011526548.1:p.Asp822Asn
XM_011528247.1:c.2464G>A	XP_011526549.1:p.Asp822Asn
XM_011528248.1:c.2761G>A	XP_011526550.1:p.Asp921Asn
XM_011528249.1:c.1435G>A	XP_011526551.1:p.Asp479Asn
XM_011528251.1:c.1018G>A	XP_011526553.1:p.Asp340Asn
XM_011528246.3:c.2464G>A	XP_011526548.1:p.Asp822Asn
XM_011528249.2:c.1435G>A	XP_011526551.1:p.Asp479Asn
XR_001753750.1:n.2918G>A
XR_001753751.1:n.2918G>A
XR_002958353.1:n.3844G>A
NM_003331.5:c.2761G>A MANE Select	NP_003322.3:p.Asp921Asn
NM_001385197.1:c.2761G>A	NP_001372126.1:p.Asp921Asn
NM_001385198.1:c.2761G>A	NP_001372127.1:p.Asp921Asn
NM_001385199.1:c.2575G>A	NP_001372128.1:p.Asp859Asn
NM_001385200.1:c.2758G>A	NP_001372129.1:p.Asp920Asn
NM_001385201.1:c.2563G>A	NP_001372130.1:p.Asp855Asn
NM_001385202.1:c.2677G>A	NP_001372131.1:p.Asp893Asn
NM_001385203.1:c.2842G>A	NP_001372132.1:p.Asp948Asn
NM_001385204.1:c.2971G>A	NP_001372133.1:p.Asp991Asn
NM_001385205.1:c.2671G>A	NP_001372134.1:p.Asp891Asn
NM_001385206.1:c.2635G>A	NP_001372135.1:p.Asp879Asn
NM_001385207.1:c.2743G>A	NP_001372136.1:p.Asp915Asn