Canonical Allele Identifier: CA403996420

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10468696C>A (hg19) ; chr19:g.10358020C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10358020C>A , CM000681.2:g.10358020C>A	GRCh38
NC_000019.9:g.10468696C>A , CM000681.1:g.10468696C>A	GRCh37
NC_000019.8:g.10329696C>A	NCBI36
NG_007872.1:g.27553G>T , LRG_121:g.27553G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*643G>T	ENSP00000514307.1:n.*643G>T
ENST00000525976.6:c.2294G>T	ENSP00000434831.2:p.Gly765Val
ENST00000527481.3:c.2294G>T	ENSP00000466340.2:p.Gly765Val
ENST00000529370.6:n.2625G>T
ENST00000529739.2:n.2708G>T
ENST00000530829.2:c.*1845G>T	ENSP00000436826.2:n.*1845G>T
ENST00000531836.6:c.2294G>T	ENSP00000436175.2:p.Gly765Val
ENST00000533334.2:c.*336G>T	ENSP00000432320.2:n.*336G>T
ENST00000534228.2:n.2708G>T
ENST00000699354.1:n.396G>T
ENST00000699355.1:c.*354G>T	ENSP00000514328.1:n.*354G>T
ENST00000699356.1:n.2708G>T
ENST00000699357.1:n.2708G>T
ENST00000699358.1:c.2294G>T	ENSP00000514329.1:p.Gly765Val
ENST00000699360.1:c.2294G>T	ENSP00000514331.1:p.Gly765Val
ENST00000525621.6:c.2294G>T MANE Select	ENSP00000431885.1:p.Gly765Val
ENST00000264818.10:c.2294G>T	ENSP00000264818.6:p.Gly765Val
ENST00000524462.5:c.1739G>T	ENSP00000433203.1:p.Gly580Val
ENST00000525621.5:c.2294G>T	ENSP00000431885.1:p.Gly765Val
ENST00000529370.5:c.2294G>T	ENSP00000432728.1:p.Gly765Val
ENST00000533334.1:c.583G>T
NM_003331.4:c.2294G>T , LRG_121t1:c.2294G>T	NP_003322.3:p.Gly765Val
XM_011528245.1:c.2294G>T	XP_011526547.1:p.Gly765Val
XM_011528246.1:c.1997G>T	XP_011526548.1:p.Gly666Val
XM_011528247.1:c.1997G>T	XP_011526549.1:p.Gly666Val
XM_011528248.1:c.2294G>T	XP_011526550.1:p.Gly765Val
XM_011528249.1:c.968G>T	XP_011526551.1:p.Gly323Val
XM_011528251.1:c.551G>T	XP_011526553.1:p.Gly184Val
XM_011528246.3:c.1997G>T	XP_011526548.1:p.Gly666Val
XM_011528249.2:c.968G>T	XP_011526551.1:p.Gly323Val
XR_001753750.1:n.2451G>T
XR_001753751.1:n.2451G>T
XR_001753752.1:n.2563G>T
XR_002958353.1:n.2332G>T
NM_003331.5:c.2294G>T MANE Select	NP_003322.3:p.Gly765Val
NM_001385197.1:c.2294G>T	NP_001372126.1:p.Gly765Val
NM_001385198.1:c.2294G>T	NP_001372127.1:p.Gly765Val
NM_001385199.1:c.2108G>T	NP_001372128.1:p.Gly703Val
NM_001385200.1:c.2294G>T	NP_001372129.1:p.Gly765Val
NM_001385201.1:c.2096G>T	NP_001372130.1:p.Gly699Val
NM_001385202.1:c.2210G>T	NP_001372131.1:p.Gly737Val
NM_001385203.1:c.2294G>T	NP_001372132.1:p.Gly765Val
NM_001385204.1:c.2294G>T	NP_001372133.1:p.Gly765Val
NM_001385205.1:c.2204G>T	NP_001372134.1:p.Gly735Val
NM_001385206.1:c.2168G>T	NP_001372135.1:p.Gly723Val
NM_001385207.1:c.2276G>T	NP_001372136.1:p.Gly759Val