Canonical Allele Identifier: CA403988693

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464849A>C (hg19) ; chr19:g.10354173A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354173A>C , CM000681.2:g.10354173A>C	GRCh38
NC_000019.9:g.10464849A>C , CM000681.1:g.10464849A>C	GRCh37
NC_000019.8:g.10325849A>C	NCBI36
NG_007872.1:g.31400T>G , LRG_121:g.31400T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1126T>G	ENSP00000514307.1:n.*1126T>G
ENST00000525976.6:c.2777T>G	ENSP00000434831.2:p.Met926Arg
ENST00000527481.3:c.2777T>G	ENSP00000466340.2:p.Met926Arg
ENST00000529370.6:n.4153T>G
ENST00000529739.2:n.3191T>G
ENST00000530829.2:c.*2328T>G	ENSP00000436826.2:n.*2328T>G
ENST00000531836.6:c.2777T>G	ENSP00000436175.2:p.Met926Arg
ENST00000533334.2:c.*819T>G	ENSP00000432320.2:n.*819T>G
ENST00000534228.2:n.4236T>G
ENST00000699354.1:n.879T>G
ENST00000699355.1:c.*1882T>G	ENSP00000514328.1:n.*1882T>G
ENST00000699356.1:n.3191T>G
ENST00000699357.1:n.4236T>G
ENST00000699358.1:c.2777T>G	ENSP00000514329.1:p.Met926Arg
ENST00000699360.1:c.2777T>G	ENSP00000514331.1:p.Met926Arg
ENST00000525621.6:c.2777T>G MANE Select	ENSP00000431885.1:p.Met926Arg
ENST00000264818.10:c.2777T>G	ENSP00000264818.6:p.Met926Arg
ENST00000524462.5:c.2222T>G	ENSP00000433203.1:p.Met741Arg
ENST00000525621.5:c.2777T>G	ENSP00000431885.1:p.Met926Arg
ENST00000527481.2:c.73T>G
ENST00000529412.1:n.449T>G
ENST00000530560.5:c.206T>G	ENSP00000465291.1:p.Met69Arg
NM_003331.4:c.2777T>G , LRG_121t1:c.2777T>G	NP_003322.3:p.Met926Arg
XM_011528245.1:c.2777T>G	XP_011526547.1:p.Met926Arg
XM_011528246.1:c.2480T>G	XP_011526548.1:p.Met827Arg
XM_011528247.1:c.2480T>G	XP_011526549.1:p.Met827Arg
XM_011528248.1:c.2777T>G	XP_011526550.1:p.Met926Arg
XM_011528249.1:c.1451T>G	XP_011526551.1:p.Met484Arg
XM_011528251.1:c.1034T>G	XP_011526553.1:p.Met345Arg
XM_011528246.3:c.2480T>G	XP_011526548.1:p.Met827Arg
XM_011528249.2:c.1451T>G	XP_011526551.1:p.Met484Arg
XR_001753750.1:n.2934T>G
XR_001753751.1:n.2934T>G
XR_002958353.1:n.3860T>G
NM_003331.5:c.2777T>G MANE Select	NP_003322.3:p.Met926Arg
NM_001385197.1:c.2777T>G	NP_001372126.1:p.Met926Arg
NM_001385198.1:c.2777T>G	NP_001372127.1:p.Met926Arg
NM_001385199.1:c.2591T>G	NP_001372128.1:p.Met864Arg
NM_001385200.1:c.2774T>G	NP_001372129.1:p.Met925Arg
NM_001385201.1:c.2579T>G	NP_001372130.1:p.Met860Arg
NM_001385202.1:c.2693T>G	NP_001372131.1:p.Met898Arg
NM_001385203.1:c.2858T>G	NP_001372132.1:p.Met953Arg
NM_001385204.1:c.2987T>G	NP_001372133.1:p.Met996Arg
NM_001385205.1:c.2687T>G	NP_001372134.1:p.Met896Arg
NM_001385206.1:c.2651T>G	NP_001372135.1:p.Met884Arg
NM_001385207.1:c.2759T>G	NP_001372136.1:p.Met920Arg