Canonical Allele Identifier: CA403995579

Gene: TYK2

Linked Data

• dbSNP Id: rs1462090710
• gnomAD v2: 19-10468516-T-G
• gnomAD v4: 19-10357840-T-G
• MyVariant Identifiers: chr19:g.10468516T>G (hg19) ; chr19:g.10357840T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10357840T>G , CM000681.2:g.10357840T>G	GRCh38
NC_000019.9:g.10468516T>G , CM000681.1:g.10468516T>G	GRCh37
NC_000019.8:g.10329516T>G	NCBI36
NG_007872.1:g.27733A>C , LRG_121:g.27733A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*739A>C	ENSP00000514307.1:n.*739A>C
ENST00000525976.6:c.2390A>C	ENSP00000434831.2:p.Lys797Thr
ENST00000527481.3:c.2390A>C	ENSP00000466340.2:p.Lys797Thr
ENST00000529370.6:n.2721A>C
ENST00000529739.2:n.2804A>C
ENST00000530829.2:c.*1941A>C	ENSP00000436826.2:n.*1941A>C
ENST00000531836.6:c.2390A>C	ENSP00000436175.2:p.Lys797Thr
ENST00000533334.2:c.*432A>C	ENSP00000432320.2:n.*432A>C
ENST00000534228.2:n.2804A>C
ENST00000699354.1:n.492A>C
ENST00000699355.1:c.*450A>C	ENSP00000514328.1:n.*450A>C
ENST00000699356.1:n.2804A>C
ENST00000699357.1:n.2804A>C
ENST00000699358.1:c.2390A>C	ENSP00000514329.1:p.Lys797Thr
ENST00000699360.1:c.2390A>C	ENSP00000514331.1:p.Lys797Thr
ENST00000525621.6:c.2390A>C MANE Select	ENSP00000431885.1:p.Lys797Thr
ENST00000264818.10:c.2390A>C	ENSP00000264818.6:p.Lys797Thr
ENST00000524462.5:c.1835A>C	ENSP00000433203.1:p.Lys612Thr
ENST00000525621.5:c.2390A>C	ENSP00000431885.1:p.Lys797Thr
ENST00000529370.5:c.2390A>C	ENSP00000432728.1:p.Lys797Thr
ENST00000529412.1:n.62A>C
ENST00000533334.1:c.679A>C
NM_003331.4:c.2390A>C , LRG_121t1:c.2390A>C	NP_003322.3:p.Lys797Thr
XM_011528245.1:c.2390A>C	XP_011526547.1:p.Lys797Thr
XM_011528246.1:c.2093A>C	XP_011526548.1:p.Lys698Thr
XM_011528247.1:c.2093A>C	XP_011526549.1:p.Lys698Thr
XM_011528248.1:c.2390A>C	XP_011526550.1:p.Lys797Thr
XM_011528249.1:c.1064A>C	XP_011526551.1:p.Lys355Thr
XM_011528251.1:c.647A>C	XP_011526553.1:p.Lys216Thr
XM_011528246.3:c.2093A>C	XP_011526548.1:p.Lys698Thr
XM_011528249.2:c.1064A>C	XP_011526551.1:p.Lys355Thr
XR_001753750.1:n.2547A>C
XR_001753751.1:n.2547A>C
XR_002958353.1:n.2428A>C
NM_003331.5:c.2390A>C MANE Select	NP_003322.3:p.Lys797Thr
NM_001385197.1:c.2390A>C	NP_001372126.1:p.Lys797Thr
NM_001385198.1:c.2390A>C	NP_001372127.1:p.Lys797Thr
NM_001385199.1:c.2204A>C	NP_001372128.1:p.Lys735Thr
NM_001385200.1:c.2390A>C	NP_001372129.1:p.Lys797Thr
NM_001385201.1:c.2192A>C	NP_001372130.1:p.Lys731Thr
NM_001385202.1:c.2306A>C	NP_001372131.1:p.Lys769Thr
NM_001385203.1:c.2390A>C	NP_001372132.1:p.Lys797Thr
NM_001385204.1:c.2390A>C	NP_001372133.1:p.Lys797Thr
NM_001385205.1:c.2300A>C	NP_001372134.1:p.Lys767Thr
NM_001385206.1:c.2264A>C	NP_001372135.1:p.Lys755Thr
NM_001385207.1:c.2372A>C	NP_001372136.1:p.Lys791Thr