Canonical Allele Identifier: CA403998389

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10468775T>G (hg19) ; chr19:g.10358099T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10358099T>G , CM000681.2:g.10358099T>G	GRCh38
NC_000019.9:g.10468775T>G , CM000681.1:g.10468775T>G	GRCh37
NC_000019.8:g.10329775T>G	NCBI36
NG_007872.1:g.27474A>C , LRG_121:g.27474A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*564A>C	ENSP00000514307.1:n.*564A>C
ENST00000525976.6:c.2215A>C	ENSP00000434831.2:p.Asn739His
ENST00000527481.3:c.2215A>C	ENSP00000466340.2:p.Asn739His
ENST00000529370.6:n.2546A>C
ENST00000529739.2:n.2629A>C
ENST00000530829.2:c.*1766A>C	ENSP00000436826.2:n.*1766A>C
ENST00000531836.6:c.2215A>C	ENSP00000436175.2:p.Asn739His
ENST00000533334.2:c.*257A>C	ENSP00000432320.2:n.*257A>C
ENST00000534228.2:n.2629A>C
ENST00000699354.1:n.317A>C
ENST00000699355.1:c.*275A>C	ENSP00000514328.1:n.*275A>C
ENST00000699356.1:n.2629A>C
ENST00000699357.1:n.2629A>C
ENST00000699358.1:c.2215A>C	ENSP00000514329.1:p.Asn739His
ENST00000699360.1:c.2215A>C	ENSP00000514331.1:p.Asn739His
ENST00000525621.6:c.2215A>C MANE Select	ENSP00000431885.1:p.Asn739His
ENST00000264818.10:c.2215A>C	ENSP00000264818.6:p.Asn739His
ENST00000524462.5:c.1660A>C	ENSP00000433203.1:p.Asn554His
ENST00000525621.5:c.2215A>C	ENSP00000431885.1:p.Asn739His
ENST00000529370.5:c.2215A>C	ENSP00000432728.1:p.Asn739His
ENST00000533334.1:c.504A>C
NM_003331.4:c.2215A>C , LRG_121t1:c.2215A>C	NP_003322.3:p.Asn739His
XM_011528245.1:c.2215A>C	XP_011526547.1:p.Asn739His
XM_011528246.1:c.1918A>C	XP_011526548.1:p.Asn640His
XM_011528247.1:c.1918A>C	XP_011526549.1:p.Asn640His
XM_011528248.1:c.2215A>C	XP_011526550.1:p.Asn739His
XM_011528249.1:c.889A>C	XP_011526551.1:p.Asn297His
XM_011528251.1:c.472A>C	XP_011526553.1:p.Asn158His
XM_011528246.3:c.1918A>C	XP_011526548.1:p.Asn640His
XM_011528249.2:c.889A>C	XP_011526551.1:p.Asn297His
XR_001753750.1:n.2372A>C
XR_001753751.1:n.2372A>C
XR_001753752.1:n.2484A>C
XR_002958353.1:n.2253A>C
NM_003331.5:c.2215A>C MANE Select	NP_003322.3:p.Asn739His
NM_001385197.1:c.2215A>C	NP_001372126.1:p.Asn739His
NM_001385198.1:c.2215A>C	NP_001372127.1:p.Asn739His
NM_001385199.1:c.2029A>C	NP_001372128.1:p.Asn677His
NM_001385200.1:c.2215A>C	NP_001372129.1:p.Asn739His
NM_001385201.1:c.2017A>C	NP_001372130.1:p.Asn673His
NM_001385202.1:c.2131A>C	NP_001372131.1:p.Asn711His
NM_001385203.1:c.2215A>C	NP_001372132.1:p.Asn739His
NM_001385204.1:c.2215A>C	NP_001372133.1:p.Asn739His
NM_001385205.1:c.2125A>C	NP_001372134.1:p.Asn709His
NM_001385206.1:c.2089A>C	NP_001372135.1:p.Asn697His
NM_001385207.1:c.2197A>C	NP_001372136.1:p.Asn733His