Canonical Allele Identifier: CA505373994

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464845C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354169C>G , CM000681.2:g.10354169C>G	GRCh38
NC_000019.9:g.10464845C>G , CM000681.1:g.10464845C>G	GRCh37
NC_000019.8:g.10325845C>G	NCBI36
NG_007872.1:g.31404G>C , LRG_121:g.31404G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.*1130G>C	ENSP00000514307.1:n.*1130G>C
ENST00000525976.6:c.2781G>C	ENSP00000434831.2:p.Val927=
ENST00000527481.3:c.2781G>C	ENSP00000466340.2:p.Val927=
ENST00000529370.6:n.4157G>C
ENST00000529739.2:n.3195G>C
ENST00000530829.2:c.*2332G>C	ENSP00000436826.2:n.*2332G>C
ENST00000531836.6:c.2781G>C	ENSP00000436175.2:p.Val927=
ENST00000533334.2:c.*823G>C	ENSP00000432320.2:n.*823G>C
ENST00000534228.2:n.4240G>C
ENST00000699354.1:n.883G>C
ENST00000699355.1:c.*1886G>C	ENSP00000514328.1:n.*1886G>C
ENST00000699356.1:n.3195G>C
ENST00000699357.1:n.4240G>C
ENST00000699358.1:c.2781G>C	ENSP00000514329.1:p.Val927=
ENST00000699360.1:c.2781G>C	ENSP00000514331.1:p.Val927=
ENST00000525621.6:c.2781G>C MANE Select	ENSP00000431885.1:p.Val927=
ENST00000264818.10:c.2781G>C	ENSP00000264818.6:p.Val927=
ENST00000524462.5:c.2226G>C	ENSP00000433203.1:p.Val742=
ENST00000525621.5:c.2781G>C	ENSP00000431885.1:p.Val927=
ENST00000527481.2:c.77G>C
ENST00000529412.1:n.453G>C
ENST00000530560.5:c.210G>C	ENSP00000465291.1:p.Val70=
NM_003331.4:c.2781G>C , LRG_121t1:c.2781G>C	NP_003322.3:p.Val927=
XM_011528245.1:c.2781G>C	XP_011526547.1:p.Val927=
XM_011528246.1:c.2484G>C	XP_011526548.1:p.Val828=
XM_011528247.1:c.2484G>C	XP_011526549.1:p.Val828=
XM_011528248.1:c.2781G>C	XP_011526550.1:p.Val927=
XM_011528249.1:c.1455G>C	XP_011526551.1:p.Val485=
XM_011528251.1:c.1038G>C	XP_011526553.1:p.Val346=
XM_011528246.3:c.2484G>C	XP_011526548.1:p.Val828=
XM_011528249.2:c.1455G>C	XP_011526551.1:p.Val485=
XR_001753750.1:n.2938G>C
XR_001753751.1:n.2938G>C
XR_002958353.1:n.3864G>C
NM_003331.5:c.2781G>C MANE Select	NP_003322.3:p.Val927=
NM_001385197.1:c.2781G>C	NP_001372126.1:p.Val927=
NM_001385198.1:c.2781G>C	NP_001372127.1:p.Val927=
NM_001385199.1:c.2595G>C	NP_001372128.1:p.Val865=
NM_001385200.1:c.2778G>C	NP_001372129.1:p.Val926=
NM_001385201.1:c.2583G>C	NP_001372130.1:p.Val861=
NM_001385202.1:c.2697G>C	NP_001372131.1:p.Val899=
NM_001385203.1:c.2862G>C	NP_001372132.1:p.Val954=
NM_001385204.1:c.2991G>C	NP_001372133.1:p.Val997=
NM_001385205.1:c.2691G>C	NP_001372134.1:p.Val897=
NM_001385206.1:c.2655G>C	NP_001372135.1:p.Val885=
NM_001385207.1:c.2763G>C	NP_001372136.1:p.Val921=