Canonical Allele Identifier: CA2322389845

Gene: TYK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10357959_10357960delinsCA , CM000681.2:g.10357959_10357960delinsCA	GRCh38
NC_000019.9:g.10468635_10468636delinsCA , CM000681.1:g.10468635_10468636delinsCA	GRCh37
NC_000019.8:g.10329635_10329636delinsCA	NCBI36
NG_007872.1:g.27613_27614delinsTG , LRG_121:g.27613_27614delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*661-42_*661-41delinsTG	ENSP00000514307.1:n.*661-42_*661-41delinsTG
ENST00000525976.6:c.2312-42_2312-41delinsTG	ENSP00000434831.2:n.2312-42_2312-41delinsTG
ENST00000527481.3:c.2312-42_2312-41delinsTG	ENSP00000466340.2:n.2312-42_2312-41delinsTG
ENST00000529370.6:n.2643-42_2643-41delinsTG
ENST00000529739.2:n.2726-42_2726-41delinsTG
ENST00000530829.2:c.*1863-42_*1863-41delinsTG	ENSP00000436826.2:n.*1863-42_*1863-41delinsTG
ENST00000531836.6:c.2312-42_2312-41delinsTG	ENSP00000436175.2:n.2312-42_2312-41delinsTG
ENST00000533334.2:c.*354-42_*354-41delinsTG	ENSP00000432320.2:n.*354-42_*354-41delinsTG
ENST00000534228.2:n.2726-42_2726-41delinsTG
ENST00000699354.1:n.414-42_414-41delinsTG
ENST00000699355.1:c.*372-42_*372-41delinsTG	ENSP00000514328.1:n.*372-42_*372-41delinsTG
ENST00000699356.1:n.2726-42_2726-41delinsTG
ENST00000699357.1:n.2726-42_2726-41delinsTG
ENST00000699358.1:c.2312-42_2312-41delinsTG	ENSP00000514329.1:n.2312-42_2312-41delinsTG
ENST00000699360.1:c.2312-42_2312-41delinsTG	ENSP00000514331.1:n.2312-42_2312-41delinsTG
ENST00000525621.6:c.2312-42_2312-41delinsTG MANE Select	ENSP00000431885.1:n.2312-42_2312-41delinsTG
ENST00000264818.10:c.2312-42_2312-41delinsTG	ENSP00000264818.6:n.2312-42_2312-41delinsTG
ENST00000524462.5:c.1757-42_1757-41delinsTG	ENSP00000433203.1:n.1757-42_1757-41delinsTG
ENST00000525621.5:c.2312-42_2312-41delinsTG	ENSP00000431885.1:n.2312-42_2312-41delinsTG
ENST00000529370.5:c.2312-42_2312-41delinsTG	ENSP00000432728.1:n.2312-42_2312-41delinsTG
ENST00000533334.1:c.601-42_601-41delinsTG
NM_003331.4:c.2312-42_2312-41delinsTG , LRG_121t1:c.2312-42_2312-41delinsTG	NP_003322.3:n.2312-42_2312-41delinsTG
XM_011528245.1:c.2312-42_2312-41delinsTG	XP_011526547.1:n.2312-42_2312-41delinsTG
XM_011528246.1:c.2015-42_2015-41delinsTG	XP_011526548.1:n.2015-42_2015-41delinsTG
XM_011528247.1:c.2015-42_2015-41delinsTG	XP_011526549.1:n.2015-42_2015-41delinsTG
XM_011528248.1:c.2312-42_2312-41delinsTG	XP_011526550.1:n.2312-42_2312-41delinsTG
XM_011528249.1:c.986-42_986-41delinsTG	XP_011526551.1:n.986-42_986-41delinsTG
XM_011528251.1:c.569-42_569-41delinsTG	XP_011526553.1:n.569-42_569-41delinsTG
XM_011528246.3:c.2015-42_2015-41delinsTG	XP_011526548.1:n.2015-42_2015-41delinsTG
XM_011528249.2:c.986-42_986-41delinsTG	XP_011526551.1:n.986-42_986-41delinsTG
XR_001753750.1:n.2469-42_2469-41delinsTG
XR_001753751.1:n.2469-42_2469-41delinsTG
XR_001753752.1:n.2581-42_2581-41delinsTG
XR_002958353.1:n.2350-42_2350-41delinsTG
NM_003331.5:c.2312-42_2312-41delinsTG MANE Select	NP_003322.3:n.2312-42_2312-41delinsTG
NM_001385197.1:c.2312-42_2312-41delinsTG	NP_001372126.1:n.2312-42_2312-41delinsTG
NM_001385198.1:c.2312-42_2312-41delinsTG	NP_001372127.1:n.2312-42_2312-41delinsTG
NM_001385199.1:c.2126-42_2126-41delinsTG	NP_001372128.1:n.2126-42_2126-41delinsTG
NM_001385200.1:c.2312-42_2312-41delinsTG	NP_001372129.1:n.2312-42_2312-41delinsTG
NM_001385201.1:c.2114-42_2114-41delinsTG	NP_001372130.1:n.2114-42_2114-41delinsTG
NM_001385202.1:c.2228-42_2228-41delinsTG	NP_001372131.1:n.2228-42_2228-41delinsTG
NM_001385203.1:c.2312-42_2312-41delinsTG	NP_001372132.1:n.2312-42_2312-41delinsTG
NM_001385204.1:c.2312-42_2312-41delinsTG	NP_001372133.1:n.2312-42_2312-41delinsTG
NM_001385205.1:c.2222-42_2222-41delinsTG	NP_001372134.1:n.2222-42_2222-41delinsTG
NM_001385206.1:c.2186-42_2186-41delinsTG	NP_001372135.1:n.2186-42_2186-41delinsTG
NM_001385207.1:c.2294-42_2294-41delinsTG	NP_001372136.1:n.2294-42_2294-41delinsTG